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Results for your request: type = DNA
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Results for dna
  Mim number
Name of disease
ICD identifier
ICD name
Nb of Families Nb of Persons Nb of patients Bank Contact Last update Date  
  302045
X-L DILATED CARDIOMYOPATHIES

3 8 3 luisa.politano@unina2.it 2008-06-30  
  278700
XERODERMA PIGMENTOSUM COMPLEMENTATION GROUP A

1 4 1 saker@genethon.fr 2008-06-26  
  278730
XERODERMA PIGMENTOSUM

15 65 23 saker@genethon.fr 2008-06-26  
 
XANTHOMATOSIS (UNDEFINED)
E78.2
Mixed hyperlipidaemia
1 1 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  194300
WOOLLY HAIR SYNDROME AUTOSOMAL DOMINANT

1 6 4 saker@genethon.fr 2008-06-26  
  222300
WOLFRAM SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
  194190
WOLF-HIRSCHHORN SYNDROME

2 6 2 saker@genethon.fr 2008-06-26  
  301000
WISKOTT-ALDRICH SYNDROME

10 13 13 saker@genethon.fr 2008-06-26  
  277900
WILSON DISEASE

4 8 3 saker@genethon.fr 2008-06-26  
  194050
WILLIAMS-BEUREN SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
  253550
WERDNIG-HOFFMANN;SMA1, SMA2

35 35 marina.fanin@unipd.it 2008-07-04  
  160500
WELANDER DISEASE

1 1 1 luisa.politano@unina2.it 2008-07-07  
  608710
WEGENER GRANULOMATOSIS
E 75.2
Wegener's Granulomatosis
1 1 1 mposada@isciii.es 2008-05-30  
  236670
WALKER-WARBURG SYNDROME

3 6 3 saker@genethon.fr 2008-06-26  
  193300
VON HIPPEL-LINDAU SYNDROME

50 159 27 saker@genethon.fr 2008-06-26  
  604117
VOHWINKEL SYNDROME

3 20 4 saker@genethon.fr 2008-06-26  
  193200
VITILIGO

4 26 9 saker@genethon.fr 2008-06-26  
  276901
USHER SYNDROME TYPE 2A

1 1 1 saker@genethon.fr 2008-06-26  
  276900
USHER SYNDROME TYPE 1A

2 6 3 saker@genethon.fr 2008-06-26  
  608149
UNIPARENTAL DISOMY, PATERNAL, CHROMOSOME 14 (UNDEFINED)
Q99.9
chromosomal aberrations unidentified
2 2 2 karcagi.veronika@oki.antsz.hu 2008-07-07  
  120220
ULRICH DISEASE

2 2 2 luisa.politano@unina2.it 2008-06-30  
  254090
ULLRICH CONGENITAL MUSCULAR DYSTROPHY

45 125 49 saker@genethon.fr 2008-06-26  
 
TUBULAR AGGREGATES
G71.2
Congenital myopathies
7 7 7 mmora@istituto-besta.it 2008-01-09  
  191100
TUBEROUS SCLEROSIS; TS

1 1 1 edith.said@um.edu.mt 2008-08-27  
  191100
TUBEROUS SCLEROSIS (UNDEFINED)
Q85.1
Tuberous sclerosis
1 1 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  191100
TUBEROUS SCLEROSIS

63 212 78 saker@genethon.fr 2008-06-26  
  275630
TRIGLYCERIDE STORAGE DISEASE

7 29 9 saker@genethon.fr 2008-06-26  
  601675
TRICHOTHIODYSTROPHY PHOTOSENSITIVE

10 45 12 saker@genethon.fr 2008-06-26  
  190345
TRICHOEPITHELIOMAS, MULTIPLE DESMOPLASTIC

2 14 5 saker@genethon.fr 2008-06-26  
  154500
TREACHER COLLINS-FRANCESCHETTI SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
 
TOXIC OIL SYNDROME

Toxic Oil Syndrome
3717 3717 mposada@isciii.es 2008-05-30  
  116700
TOTAL CONGENITAL CATARACT

2 4 2 saker@genethon.fr 2008-06-26  
  128100
TORSION DYSTONIA

1 2 saker@genethon.fr 2008-06-26  
  162500
TOMACULOUS NEUROPATHY

1 1 1 saker@genethon.fr 2008-06-26  
 
THOMSEN/BECKER DISEASE CLCN1 CHANNEL
G71.1
Myotonic disorders
50 58 58 mmora@istituto-besta.it 2008-01-09  
  160800
THOMSEN BECKER DISEASE CLCN1 CHANNEL

2 maurizio.moggio@unimi.it 2008-06-23  
  272800
TAY-SACHS DISEASE

2 10 2 saker@genethon.fr 2008-06-26  
  152700
SYSTEMIC LUPUS ERYTHEMATOSUS

3 7 6 saker@genethon.fr 2008-06-26  
  186700
SYRINGOMYELIA
G 95.0
Syringomyelia
1 1 1 mposada@isciii.es 2008-05-30  
  601887
SUSCEPTIBILITY TO MALIGNANT HYPERTHERMIA 5

3 9 saker@genethon.fr 2008-06-26  
  600467
SUSCEPTIBILITY TO MALIGNANT HYPERTHERMIA 4

7 10 saker@genethon.fr 2008-06-26  
  154276
SUSCEPTIBILITY TO MALIGNANT HYPERTHERMIA 3

5 7 saker@genethon.fr 2008-06-26  
  154275
SUSCEPTIBILITY TO MALIGNANT HYPERTHERMIA 2

36 133 4 saker@genethon.fr 2008-06-26  
  145600
SUSCEPTIBILITY TO MALIGNANT HYPERTHERMIA 1

57 132 113 saker@genethon.fr 2008-06-26  
 
SUDECK'S DYSTROPHY
M 89.0
Sudeck's dystrophy
1 1 1 mposada@isciii.es 2008-05-30  
  601559
STUVE-WIEDEMANN SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
  185300
STURGE-WEBER SYNDROME ( UNDEFINED)

1 1 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  184500
STEATOCYSTOMA MULTIPLEX

6 16 6 saker@genethon.fr 2008-06-26  
  183600
SPLIT-HAND/FOOT DEFORMITY 1

1 2 1 saker@genethon.fr 2008-06-26  
 
SPINOCEREBELLAR/CEREBELLAR ATAXIA
G11
Hereditary ataxia
12 12 12 mmora@istituto-besta.it 2008-01-09  
  109150
SPINOCEREBELLAR ATAXIA, SCA1, SCA2, SCA6, SCA8, SCA7, SCA5, SCA19, SCA10, SCA17, SCA12, SCA27, SCA25, SCA21, SCA16, SCA14, SCA15 (UNDEFINED)
G11.1
Early-onset cerebellar ataxia
12 20 11 karcagi.veronika@oki.antsz.hu 2008-07-07  
  164400
SPINOCEREBELLAR ATAXIA 1

5 20 9 saker@genethon.fr 2008-06-26  
  164400
SPINOCEREBELLAR ATAXIA

14 59 19 saker@genethon.fr 2008-06-26  
  253400
SPINAL MUSCULAR ATROPHY, TYPE II-III; SMA2-3
G12.1
Other inherited spinal muscular atrophy (type II- III [Kugelberg-Welander])
50 120 47 luisa.politano@unina2.it 2008-06-30  
  253550
SPINAL MUSCULAR ATROPHY, SMA-1,2,3
G12
Spinal muscular atrophy and related syndromes
84 84 84 mmora@istituto-besta.it 2008-01-09  
  253550
SPINAL MUSCULAR ATROPHY, SMA-1,2,3

52 maurizio.moggio@unimi.it 2008-06-23  
  604320
SPINAL MUSCULAR ATROPHY WITH RESPIRATORY DISTRESS 1; SMARD1 (DEFINED)
G12
Spinal muscular atrophy and related syndromes
1 5 2 karcagi.veronika@oki.antsz.hu 2008-07-07  
  182980
SPINAL MUSCULAR ATROPHY PROXIMAL

56 60 3 saker@genethon.fr 2008-06-26  
  253300
SPINAL MUSCULAR ATROPHY 1

219 544 269 saker@genethon.fr 2008-06-26  
  253300
SPINAL MUSCULAR ATROPHY (UNDEFINED)
G12.0 G12.1 G12.1
Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] Other inherited spinal muscular atrophy Other inherited spinal muscular atrophy G 12.1 Spinal muscular atrophy and related syndromes
291 461 291 karcagi.veronika@oki.antsz.hu 2008-07-07  
  253300
SPINAL MUSCULAR ATROPHY (DEFINED)
G12.0 G12.1 G12.1
Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] Other inherited spinal muscular atrophy Other inherited spinal muscular atrophy G 12.1 Spinal muscular atrophy and related syndromes
244 797 264 karcagi.veronika@oki.antsz.hu 2008-07-07  
  313200
SPINAL BULBAR MUSCULAR ATROPHY, KENNEDY
G12.8
Other spinal muscular atrophies and related syndromes
6 6 6 mmora@istituto-besta.it 2008-01-09  
  313200
SPINAL BULBAR ATROPHY, KENNEDY

4 maurizio.moggio@unimi.it 2008-06-23  
  313200
SPINAL AND BULBAR MUSCULAR ATROPHY, X-LINKED 1; SMAX1
G12.1
Other spinal muscular atrophies and related syndromes (spinobulbar form, Type Kennedy)
2 9 7 luisa.politano@unina2.it 2008-06-30  
  312910
SPASTICUS PARAPARESIS

4 4 4 karcagi.veronika@oki.antsz.hu 2008-07-07  
  182601
SPASTICA PARAPLEGIA, SPG4

8 8 marina.fanin@unipd.it 2008-07-04  
  607259
SPASTIC PARAPLEGIA AD/ AR

227 1274 517 saker@genethon.fr 2008-06-26  
  182601
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE; SPG4
G11.4
Hereditary spastic paraplegia
2 8 8 luisa.politano@unina2.it 2008-06-30  
  182600
SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A,
G 11.4
Strumpell-Lorrain syndrome
2 2 2 mposada@isciii.es 2008-05-30  
  602783
SPASTIC PARAPARESIS (PARAPLEGIN. DEF.)

8 maurizio.moggio@unimi.it 2008-06-23  
  602783
SPASTIC PARAPARESIS (PARAPLEGIN DEF.)
G11.4
Hereditary spastic paraplegia
2 6 6 mmora@istituto-besta.it 2008-01-09  
  270550
SPASTIC ATAXIA; SACS

4 4 marina.fanin@unipd.it 2008-07-04  
  270550
SPASTIC ATAXIA CHARLEVOIX-SAGUENAY TYPE

2 12 5 saker@genethon.fr 2008-06-26  
  270550
SPASTIC ATAXIA
G 11.4
Hereditary spastic paraplegia
5 5 5 mposada@isciii.es 2008-05-30  
  117550
SOTOS SYNDROME

2 5 3 saker@genethon.fr 2008-06-26  
  182290
SMITH-MAGENIS SYNDROME

6 19 6 saker@genethon.fr 2008-06-26  
  270300
SKIN PEELING? FAMILIAL CONTINUOUS

2 9 3 saker@genethon.fr 2008-06-26  
  270200
SJOGREN-LARSSON SYNDROME

3 7 3 saker@genethon.fr 2008-06-26  
  270100
SITUS INVERSUS VISCERUM

1 3 1 saker@genethon.fr 2008-06-26  
  260400
SHWACHMAN-DIAMOND SYNDROME; SDS

Schwasman syndrome
1 2 2 mposada@isciii.es 2008-05-30  
  260400
SHWACHMAN-DIAMOND SYNDROME (UNDEFINED)

1 3 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  607208
SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI (UNDEFINED)
G40.3
Generalized idiopathic epilepsy and epileptic syndromes
15 44 15 karcagi.veronika@oki.antsz.hu 2008-07-07  
  607208
SEVERE MYOCLONIC EPILEPSY OF INFANCY; SMEI (DEFINED)
G40.3
Generalized idiopathic epilepsy and epileptic syndromes
17 48 17 karcagi.veronika@oki.antsz.hu 2008-07-07  
  607208
SEVERE MYOCLONIC EPILEPSY OF INFANCY

109 360 124 saker@genethon.fr 2008-06-26  
  182125
SEPIAPTERIN REDUCTASE; SPR

5 17 7 edith.said@um.edu.mt 2008-08-27  
  269500
SCLEROSTEOSIS

1 4 1 saker@genethon.fr 2008-06-26  
  181750
SCLERODERMA
M 34
Scleroderma
2 2 2 mposada@isciii.es 2008-05-30  
  255800
SCHWARTZ-JAMPEL SYNDROME

11 27 13 saker@genethon.fr 2008-06-26  
  181500
SCHIZOPHRENIA

107 437 184 saker@genethon.fr 2008-06-26  
  269160
SCHIZENCEPHALY

1 1 1 saker@genethon.fr 2008-06-26  
 
SCAPULO-PERONEAL DYSTROPHY
G71.0
Muscular dystrophy
23 23 23 mmora@istituto-besta.it 2008-01-09  
  181000
SARCOIDOSIS
D 86
Sarcoidosis
1 1 1 mposada@isciii.es 2008-05-30  
  211390
SABINAS BRITTLE HAIR SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
 
S. OF DOWN

186 maurizio.moggio@unimi.it 2008-06-23  
  107970
RVAD

2 20 2 luisa.politano@unina2.it 2008-06-30  
  180849
RUBINSTEIN-TAYBI SYNDROME

38 43 36 saker@genethon.fr 2008-06-26  
  268400
ROTHMUND-THOMSON SYNDROME

4 9 5 saker@genethon.fr 2008-06-26  
  268300
ROBERTS SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
  606072
RIPPLING MUSCLE DISEASE

2 2 2 saker@genethon.fr 2008-06-26  
  602771
RIGID SPINE MUSCULAR DYSTROPHY (UNDEFINED)

1 1 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  602771
RIGID SPINE MUSCULAR DYSTROPHY

22 55 22 saker@genethon.fr 2008-06-26  
  312750
RETT SYNDROME (UNDEFINED)
F84.2
Rett's syndrome
1 6 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  312750
RETT SYNDROME

112 435 108 saker@genethon.fr 2008-06-26  
  312700
RETINOSCHISIS 1

13 14 14 saker@genethon.fr 2008-06-26  
  180200
RETINOBLASTOMA; RB1

2 3 3 edith.said@um.edu.mt 2008-08-27  
  180200
RETINOBLASTOMA RB1 (UNDEFINED)
H54.0
Blidness, both eyes
2 5 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  180200
RETINOBLASTOMA

2 2 1 saker@genethon.fr 2008-06-26  
  268000
RETINITIS PIGMENTOSA; RP (UNDEFINED)
H35.5
Hereditary retinal dystrophy
1 1 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  268000
RETINITIS PIGMENTOSA

13 42 19 saker@genethon.fr 2008-06-26  
  179850
RETICULAR PIGMENTED ANOMALY OF FLEXURES

1 3 2 saker@genethon.fr 2008-06-26  
 
RESPIRATORY CHAIN DEFECTS
G71.3
Mitochondrial myopathy, not elsewhere classified
140 158 158 mmora@istituto-besta.it 2008-01-09  
  266500
REFSUM DISEASE

2 8 3 saker@genethon.fr 2008-06-26  
  177900
PSORIASIS

202 2071 816 saker@genethon.fr 2008-06-26  
  177850
PSEUDOXANTOMA ELASTICUM

4 14 3 saker@genethon.fr 2008-06-26  
  602668
PROXIMAL MYOTONIC MYOPATHY

47 63 48 saker@genethon.fr 2008-06-26  
  177000
PROTOPORPHYRIA ERYTHROPOIETIC

3 5 3 saker@genethon.fr 2008-06-26  
  176920
PROTEUS SYNDROME

2 2 2 saker@genethon.fr 2008-06-26  
  176100
PROPHYRIA CUTANEA TARDA

2 2 2 saker@genethon.fr 2008-06-26  
  248700
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA
H49.4
Progressive external ophthalmoplegia (CPEO)
5 5 5 luisa.politano@unina2.it 2008-06-30  
  137750
PRIMARY OPEN ANGLE GLAUCOMA

2 11 4 saker@genethon.fr 2008-06-26  
  176270
PRADER-WILLY SYNDROME (PWS) (UNDEFINED)
Q87.1
Hypothalamic dysfunction, not elsewhere classified
1 1 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  176270
PRADER-WILLI SYNDROME; PWS
Q 87.1
Prader Willi syndrome
1 1 1 mposada@isciii.es 2008-05-30  
  175850
POROKERATOSIS PLANTARIS? PALMARIS ET DISSEMINATA

2 4 3 saker@genethon.fr 2008-06-26  
 
POLYMYOSITIS
M33.2
Polymyositis
69 69 69 mmora@istituto-besta.it 2008-01-09  
 
POLYMYOSISTIS
K 22.6
Polymyosistis
3 3 3 mposada@isciii.es 2008-05-30  
  173900
POLYCYSTIC KIDNEYS (UNDEFINED)
N17-N19
Renal failure
1 1 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  173900
POLYCISTIC KIDNEY; AUTOSOMAL DOMINANT

2 10 2 luisa.politano@unina2.it 2008-06-30  
 
PLANE LIQUEN
G 71.2
Plane Liquen
1 1 1 mposada@isciii.es 2008-05-30  
  173200
PITYRIASIS RUBRA PILARIS

1 5 2 saker@genethon.fr 2008-06-26  
  301220
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS

1 4 saker@genethon.fr 2008-06-26  
  261630
PHENYLKETONURIA II

3 11 4 edith.said@um.edu.mt 2008-08-27  
  261540
PETERS-PLUS SYNDROME

1 3 1 saker@genethon.fr 2008-06-26  
  601152
PERIPHERAL NEUROPATHY AND OPTIC ATROPHY

4 9 5 saker@genethon.fr 2008-06-26  
  142680
PERIODIC FEVER, FAMILIAL (UNDEFINED)

1 1 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
 
PEO/KSS
G71.3
Mitochondrial myopathy, not elsewhere classified
90 107 107 mmora@istituto-besta.it 2008-01-09  
  530000
PEO, KSS
G71.3
3 3 marina.fanin@unipd.it 2008-07-04  
 
PEO 3243 POINT MUTATIONS

8 maurizio.moggio@unimi.it 2008-06-23  
  208150
PENA-SHOKEIR SYN DROME

1 1 1 saker@genethon.fr 2008-06-26  
  312080
PELIZAEUS-MERZBACHER SYNDROME (PMD) (UNDEFINED)
G36
Other acut disseminated demyelinisation
2 5 3 karcagi.veronika@oki.antsz.hu 2008-07-07  
  312080
PELIZAEUS-MERZBACHER DISEASE

3 8 4 saker@genethon.fr 2008-06-26  
 
PEHO SYNDROME (UNDEFINED)
H47.2 G93.4
Optic atrophy, progressive encephalopathy, edema
1 12 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  311770
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA, INCLUDED
D 59.5
Nocturnal paroxistic hemoglobinuria
1 1 1 mposada@isciii.es 2008-05-30  
  311770
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA

1 1 1 saker@genethon.fr 2008-06-26  
  168600
PARKINSON DISEASE; PD

200 200 200 edith.said@um.edu.mt 2008-08-27  
  168000
PARAGANGLIOMAS 1

1 11 4 saker@genethon.fr 2008-06-26  
  245000
PAPILLON-LEFEVRE SYNDROME

14 58 24 saker@genethon.fr 2008-06-26  
  144200
PALMOPLANTAR KERATODERMA VORNER TYPE

1 35 16 saker@genethon.fr 2008-06-26  
  600962
PALMOPLANTAR KERATODERMA NONEPIDERMOLYTIC UNNA-THOST DISEASE

1 12 7 saker@genethon.fr 2008-06-26  
  167210
PACHYONYCHIA CONGENITA? JACKSON-LAMLER TYPE

1 6 4 saker@genethon.fr 2008-06-26  
  167200
PACHYONYCHIA CONGENITA TYPE 1

1 10 1 saker@genethon.fr 2008-06-26  
 
OTHER MTDNA POINT MUTATIONS

42 maurizio.moggio@unimi.it 2008-06-23  
 
OTHER MITOCHONDRIAL DISORDERS

208 maurizio.moggio@unimi.it 2008-06-23  
 
OTHER LGMD

54 maurizio.moggio@unimi.it 2008-06-23  
  166710
OSTEOPOROSIS

504 689 178 saker@genethon.fr 2008-06-26  
  259250
OSTEODYSPLASIA FAMILIAL

1 1 1 saker@genethon.fr 2008-06-26  
  119530
OROFACIAL CLEFT 1

1 18 3 saker@genethon.fr 2008-06-26  
  165500
OPTIC ATROPHY; OPA1
G71.3
2 2 marina.fanin@unipd.it 2008-07-04  
  165500
OPTIC ATROPHY 1; OPA1 (UNDEFINED)
H47.2
Optic atrophy
1 1 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  300000
OPITZ SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
  258100
OGUCHI DISEASE

1 3 1 saker@genethon.fr 2008-06-26  
  164300
OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD (UNDEFINED)
G71.0
Muscular dystrophy
1 1 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  164300
OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD (DEFINED)
G71.0
Muscular dystrophy
1 1 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  164300
OCULOPHARYNGEAL MUSCULAR DYSTROPHY

143 301 191 saker@genethon.fr 2008-06-26  
  164300
OCULOPHARYNGEAL MD, OPMD

1 1 1 luisa.politano@unina2.it 2008-07-07  
  164300
OCULO-PHARYNGEAL DYSTROPHY
G71.0
Muscular dystrophy
22 22 22 mmora@istituto-besta.it 2008-01-09  
  164300
OCULO-PHARYNGEAL

3 maurizio.moggio@unimi.it 2008-06-23  
  164210
OCULOAURICULOVERTEBRAL DYSPLASIA-GOLDENHAR SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
  602025
OBESITY

227 429 13 saker@genethon.fr 2008-06-26  
  310600
NORRIE DISEASE; NDP (DEFINED)
H35.0
Background retinopathy and retinal vascular changes
1 20 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  605275
NOONAN SYNDROME 2

2 12 4 saker@genethon.fr 2008-06-26  
  162500
NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP (UNDEFINED)
G60.0
Hereditary motor and sensory neuropathy
5 6 5 karcagi.veronika@oki.antsz.hu 2008-07-07  
  162500
NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP (DEFINED)
G60.0
Hereditary motor and sensory neuropathy
6 14 10 karcagi.veronika@oki.antsz.hu 2008-07-07  
  223900
NEUROPATHY HEREDITARY SENSORY AND AUTONOMIC TYPE III

1 1 1 saker@genethon.fr 2008-06-26  
  551500
NEUROPATHY ATAXIA AND RETINITIS PIGMENTOSA

1 3 2 saker@genethon.fr 2008-06-26  
  607379
NEUROFIBROMIN 2

1 1 1 saker@genethon.fr 2008-06-26  
  162200
NEUROFIBROMATOSIS, TYPE I; NF1

2 4 1 edith.said@um.edu.mt 2008-08-27  
  162200
NEUROFIBROMATOSIS 1

1 1 1 luisa.politano@unina2.it 2008-07-07  
  162200
NEUROFIBROMATOSIS

14 20 13 saker@genethon.fr 2008-06-26  
  256600
NEUROAXONAL DYSTROPHY INFANTILE

3 9 6 saker@genethon.fr 2008-06-26  
  256500
NETHERTON SYNDROME

9 36 10 saker@genethon.fr 2008-06-26  
  194070
NEPHROBLASTOMA

15 18 16 saker@genethon.fr 2008-06-26  
  256030
NEMALINE MYOPATHY; NEM2

3 3 marina.fanin@unipd.it 2008-07-04  
  161800
NEMALINE MYOPATHY 3; NEM3 (UNDEFINED)
G72.9
other myopathies
2 6 2 karcagi.veronika@oki.antsz.hu 2008-07-07  
  161800
NEMALINE MYOPATHY 3; NEM3 (DEFINED)
G72.9
other myopathies
2 2 2 karcagi.veronika@oki.antsz.hu 2008-07-07  
 
NEMALINE MYOPATHY
G71.2
Congenital myopathies
14 14 14 mmora@istituto-besta.it 2008-01-09  
  161800
NEMALINE MYOPATHY

112 341 133 saker@genethon.fr 2008-06-26  
  551500
NARP

3 maurizio.moggio@unimi.it 2008-06-23  
  310400
MYOTUBULAR MYOPATHY, MTMX
G71.2
Congenital myopathies
1 1 1 mmora@istituto-besta.it 2008-01-09  
  310400
MYOTUBULAR MYOPATHY 1; MTM1
G71.2
Congenital myopathies (Myotubular myopathy, x-linked)
1 7 3 luisa.politano@unina2.it 2008-06-30  
  310400
MYOTUBULAR MYOPATHY

27 105 25 saker@genethon.fr 2008-06-26  
  160900
MYOTONIC DYSTROPHY;DM1

1 1 1 edith.said@um.edu.mt 2008-08-27  
  160900
MYOTONIC DYSTROPHY;DM1
G71.1
75 75 marina.fanin@unipd.it 2008-07-04  
  602668
MYOTONIC DYSTROPHY; DM2
G71.1
11 11 marina.fanin@unipd.it 2008-07-04  
  160900
MYOTONIC DYSTROPHY, STEINERT, DM1
G71.1
Myotonic disorders
70 204 140 mmora@istituto-besta.it 2008-01-09  
  160900
MYOTONIC DYSTROPHY, STEINERT, DM1

21 maurizio.moggio@unimi.it 2008-06-23  
  602668
MYOTONIC DYSTROPHY TYPE 2, PROMM, DM2
G71.1
Myotonic disorders
5 5 5 mmora@istituto-besta.it 2008-01-09  
  255700
MYOTONIA CONGENITA, AUTOSOMAL-RECESSIVE
G71.1
Recessive myotonia congenita (Becker)
1 1 luisa.politano@unina2.it 2008-06-30  
  160800
MYOTONIA CONGENITA- THOMSEN DISEASE

67 103 76 saker@genethon.fr 2008-06-26  
  160565
MYOPATHY, TUBULAR AGGEGATES
G71.3
Mitochondrial Myopathy (with tubular aggregates)
1 1 1 luisa.politano@unina2.it 2008-06-30  
  160150
MYOPATHY, CENTRONUCLEAR (UNDEFINED)
G71.2
Congenital myopathies
1 5 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  310440
MYOPATHY WITH EXCESSIVE AUTOPHAGY

2 3 3 saker@genethon.fr 2008-06-26  
  102770
MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY

1 1 1 saker@genethon.fr 2008-06-26  
  160500
MYOPATHY DISTAL 1

1 4 3 saker@genethon.fr 2008-06-26  
  160300
MYOPATHY DISTAL

161 322 185 saker@genethon.fr 2008-06-26  
  601419
MYOPATHY DESMIN RELATED

32 136 52 saker@genethon.fr 2008-06-26  
  158810
MYOPATHY BENIGN CONGENITAL WITH CONTRACTURES

28 70 38 saker@genethon.fr 2008-06-26  
 
MYOFIBRILLAR MYOPATHIES

maurizio.moggio@unimi.it 2008-06-23  
  254780
MYOCLONIC EPILEPSY OF LAFORA

15 58 16 saker@genethon.fr 2008-06-26  
  545000
MYOCLONIC EPILEPSY (UNDEFINED)
G40.3
Generalized idiopathic epilepsy and epileptic syndromes
2 2 2 karcagi.veronika@oki.antsz.hu 2008-07-07  
  254200
MYASTHENIA GRAVIS

638 1430 637 saker@genethon.fr 2008-06-26  
 
MYASTHENIA GRAVIS
G70.0
Myasthenia gravis
110 110 110 mmora@istituto-besta.it 2008-01-09  
 
MYASTENIC SYNDROME
G70.2
Congenital and developmental myasthenia
2 4 2 mmora@istituto-besta.it 2008-01-09  
  607155
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I
G71.0
Muscular dystrophy (LGMD 2H with mutation inTRIM32)
5 9 5 luisa.politano@unina2.it 2008-06-30  
  607155
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2I; LGMD2I
G71.0
Muscular dystrophy (LGMD 2I with mutation in FKRP)
11 39 14 luisa.politano@unina2.it 2008-06-30  
  608099
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2F; LGMD2F
G71.0
Muscular dystrophy (LGMD 2F with mutation in delta-SG)
1 12 2 luisa.politano@unina2.it 2008-06-30  
  608099
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E; LGMD2E
G71.0
Muscular dystrophy (LGMD 2E with mutation in beta-SG)
5 6 6 luisa.politano@unina2.it 2008-06-30  
  608099
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2D; LGMD2D
G71.0
Muscular dystrophy (LGMD 2D with mutation in alpha-SG)
3 13 5 luisa.politano@unina2.it 2008-06-30  
  253700
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C
G71.0
Muscular dystrophy (LGMD 2C with mutation in gamma-SG)
12 36 20 luisa.politano@unina2.it 2008-06-30  
  253601
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B; LGMD2B
G71.0
Muscular dystrophy (LGMD 2B)
24 29 24 luisa.politano@unina2.it 2008-06-30  
  253600
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A
G71.0
Muscular dystrophy (LGMD 2A)
93 102 100 luisa.politano@unina2.it 2008-06-30  
  607801
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1C; LGMD1C
G71.0
Muscular dystrophy (LGMD 1C)
5 5 5 luisa.politano@unina2.it 2008-06-30  
  159001
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B; LGMD1B
G71.0
Muscular dystrophy (LGMD 1B)
11 13 13 luisa.politano@unina2.it 2008-06-30  
  253700
MUSCULAR DYSTROPHY, LIMB-GIRDLE TYPE 2C

47 164 86 saker@genethon.fr 2008-06-26  
  253600
MUSCULAR DYSTROPHY, LIMB-GIRDLE TYPE 2A

63 370 119 saker@genethon.fr 2008-06-26  
  607801
MUSCULAR DYSTROPHY, LIMB-GIRDLE TYPE 1C

5 5 5 saker@genethon.fr 2008-06-26  
  310200
MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD
G71.0
Muscular dystrophy (Duchenne type with known mutation)
491 561 561 luisa.politano@unina2.it 2008-06-30  
  310200
MUSCULAR DYSTROPHY, DUCHENNE TYPE, DMD
G 71.0
Muscular Dystrophy
2 2 2 mposada@isciii.es 2008-05-30  
  607855
MUSCULAR DYSTROPHY, CONGENITAL MEROSIN-DEFICIENT, 1A; MDC1A
G71.2
Congenital myopathies (Muscular Dystrophy with primary Merosinopathy)
3 12 3 luisa.politano@unina2.it 2008-06-30  
  310100
MUSCULAR DYSTROPHY, BECKER TYPE; BMD
G71.0
Muscular dystrophy (Becker type with known mutation)
146 174 174 luisa.politano@unina2.it 2008-06-30  
  310200
MUSCULAR DYSTROPHY DUCHENNE TYPE

56 86 58 saker@genethon.fr 2008-06-26  
  300376
MUSCULAR DYSTROPHY BECKER TYPE

25 37 27 saker@genethon.fr 2008-06-26  
  253280
MUSCLE-EYE-BRAIN DISEASE

4 9 3 saker@genethon.fr 2008-06-26  
  186600
MULTIPLE SYRINGOMAS

2 7 3 saker@genethon.fr 2008-06-26  
  126200
MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO; MS

65 65 65 edith.said@um.edu.mt 2008-08-27  
  126200
MULTIPLE SCLEROSIS

38 236 88 saker@genethon.fr 2008-06-26  
  255320
MULTIMINICORE DISEASE

96 311 106 saker@genethon.fr 2008-06-26  
  191900
MUCKLE-WELLS SYNDROME

5 26 12 saker@genethon.fr 2008-06-26  
 
MTDNA MULTIPLE DELETIONS

130 maurizio.moggio@unimi.it 2008-06-23  
 
MTDNA MACRODELETIONS

9 maurizio.moggio@unimi.it 2008-06-23  
 
MTDNA DEPLETION

15 maurizio.moggio@unimi.it 2008-06-23  
  157900
MOEBIUS SYNDROME

2 2 2 saker@genethon.fr 2008-06-26  
 
MITOCHONDRIAL-LIPID-GLYCOGEN STORAGE
G71.3
Mitochondrial myopathy, not elsewhere classified
1 1 1 mmora@istituto-besta.it 2008-01-09  
  540000
MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS, MERRF, LEIGH, COX (UNDEFINED)
G71.3
Mitochondrial myopathy, not elsewhere classified
108 139 117 karcagi.veronika@oki.antsz.hu 2008-07-07  
  540000
MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS, MERRF, LEIGH (DEFINED)
G71.3
Mitochondrial myopathy, not elsewhere classified
10 18 9 karcagi.veronika@oki.antsz.hu 2008-07-07  
  251900
MITOCHONDRIAL MYOPATHY

25 42 31 saker@genethon.fr 2008-06-26  
  255320
MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA (UNDEFINED)
G71.2
Congenital myopathies
2 6 4 karcagi.veronika@oki.antsz.hu 2008-07-07  
 
MINICORE MYOPATHY
G71.2
Congenital myopathies
7 7 7 mmora@istituto-besta.it 2008-01-09  
  255320
MINICORE DISEASE

1 1 1 luisa.politano@unina2.it 2008-06-30  
 
MILD NON SPECIFIC MYOPATHIC SIGNS

777 maurizio.moggio@unimi.it 2008-06-23  
  251200
MICROCEPHALY

3 3 3 saker@genethon.fr 2008-06-26  
  250100
METACHROMATIC LEUKODYSTROPHY

2 8 3 saker@genethon.fr 2008-06-26  
  545000
MERRF

38 maurizio.moggio@unimi.it 2008-06-23  
  545000
MERRF
G71.3
2 2 marina.fanin@unipd.it 2008-07-04  
  156225
MEROSINOPATHY;LAMA2
G71.0
23 23 marina.fanin@unipd.it 2008-07-04  
  607855
MEROSINOPATHY, LAMA2
G71.2
Congenital myopathies
21 22 22 mmora@istituto-besta.it 2008-01-09  
  309400
MENKES DISEASE

2 4 2 saker@genethon.fr 2008-06-26  
 
MELAS/MERRF
G71.3
Mitochondrial myopathy, not elsewhere classified
37 37 37 mmora@istituto-besta.it 2008-01-09  
  540000
MELAS

38 maurizio.moggio@unimi.it 2008-06-23  
  540000
MELAS
G71.3
45 45 marina.fanin@unipd.it 2008-07-04  
  604004
MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS

27 125 29 saker@genethon.fr 2008-06-26  
  232600
MC ARDLE DISEASE

16 16 marina.fanin@unipd.it 2008-07-04  
  248800
MARINESCO-SJOGREN SYNDROME

3 14 8 saker@genethon.fr 2008-06-26  
 
MARINESCO SJOGREN SYNDROME/CCFDN (UNDEFINED)
M62.5
Muscle wasting and atrophy, not elsewhere classified
4 8 5 karcagi.veronika@oki.antsz.hu 2008-07-07  
 
MARINESCO SJOGREN SYNDROME/CCFDN (DEFINED)
M62.5
Muscle wasting and atrophy, not elsewhere classified
2 5 2 karcagi.veronika@oki.antsz.hu 2008-07-07  
  154700
MARFAN SYNDROME

9 13 12 saker@genethon.fr 2008-06-26  
  248700
MARDEN-WALKER SYNDROME

1 2 2 saker@genethon.fr 2008-06-26  
  125480
MANIC-DEPRESSIVE PSYCHOSIS

49 199 81 saker@genethon.fr 2008-06-26  
  145600
MALIGNANT HYPERTHERMIA;MH

2 2 marina.fanin@unipd.it 2008-07-04  
  117000
MALIGNANT HYPERTHERMIA, CCD;MH

1 1 marina.fanin@unipd.it 2008-07-04  
 
MALIGNANT HYPERTHERMIA

192 maurizio.moggio@unimi.it 2008-06-23  
  145600
MALIGNANT HYPERTHERMIA
T88.3
Malignant hyperthermia
3 3 3 luisa.politano@unina2.it 2008-06-30  
  248300
MAL DE MELEDA

48 304 93 saker@genethon.fr 2008-06-26  
 
MAD DEFICIENCY

6 maurizio.moggio@unimi.it 2008-06-23  
  153700
MACULAR DYSTROPHY, VITELLIFORM

1 4 1 saker@genethon.fr 2008-06-26  
  109150
MACHADO JOSEPH DISEASE, MJD

1 1 1 mposada@isciii.es 2008-05-30  
  247200
LYSSENCEPHALIA (MDLS) (UNDEFINED)
G30-G32
Other degenerative disease of the nervous system
1 2 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  308240
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED (UNDEFINED)
D47.9
Neoplasm of uncertain or unknown behaviour of lymphoid, haematopoietic and related tissue, unspecified
1 4 4 karcagi.veronika@oki.antsz.hu 2008-07-07  
  152460
LOBULAR GLOMERULOPATHY FAMILIAL

1 28 9 saker@genethon.fr 2008-06-26  
  607432
LISSENCEPHALY

9 21 4 saker@genethon.fr 2008-06-26  
  151800
LIPOMATOSIS, FAMILIAL BENIGN CERVICAL
E 88.2
Lipomatosis
1 1 1 mposada@isciii.es 2008-05-30  
  151900
LIPOMATOSIS MULTIPLE

1 1 1 saker@genethon.fr 2008-06-26  
  608056
LIPOATROPHY WITH DIABETES HEPATIC STEATOSIS

1 2 2 saker@genethon.fr 2008-06-26  
 
LIPID STORAGE MYOPATHY
E75.6
Lipid storage disorder, unspecified
40 40 40 mmora@istituto-besta.it 2008-01-09  
 
LIPID STORAGE MYOPATHY

4 maurizio.moggio@unimi.it 2008-06-23  
  255100
LIPID STORAGE MYOPATHY

9 9 9 luisa.politano@unina2.it 2008-06-30  
  607155
LIMB-GIRDLE DYSTROPHY 2I;LGMD2I
G71.0
51 51 marina.fanin@unipd.it 2008-07-04  
  535000
LHON-LEBER OPTIC ATROPHY (UNDEFINED)
H47.2
Optic atrophy
120 161 132 karcagi.veronika@oki.antsz.hu 2008-07-07  
  535000
LHON-LEBER OPTIC ATROPHY (DEFINED)
H47.2
Optic atrophy
22 55 36 karcagi.veronika@oki.antsz.hu 2008-07-07  
  607155
LGMD2I, FKRP

8 maurizio.moggio@unimi.it 2008-06-23  
  607155
LGMD2I, FKRP
G71.0
Muscular dystrophy
4 5 5 mmora@istituto-besta.it 2008-01-09  
  601287
LGMD2F, DELTA-SARCOGLYCANOPATHY

maurizio.moggio@unimi.it 2008-06-23  
  604286
LGMD2E, BETA-SARCOGLYCANOPATHY

9 maurizio.moggio@unimi.it 2008-06-23  
  604286
LGMD2E, BETA-SARCOGLYCANOPATHY
G71.0
Muscular dystrophy
4 5 5 mmora@istituto-besta.it 2008-01-09  
  600899
LGMD2D, ALPHA-SARCOGLYCANOPATHY
G71.0
Muscular dystrophy
6 6 6 mmora@istituto-besta.it 2008-01-09  
  600899
LGMD2D, ALPHA-SARCOGLYCANOPATHY

12 maurizio.moggio@unimi.it 2008-06-23  
  253700
LGMD2C, GAMMA-SARCOGLYCANOPATHY

4 maurizio.moggio@unimi.it 2008-06-23  
  253700
LGMD2C, GAMMA-SARCOGLYCANOPATHY
G71.0
Muscular dystrophy
4 7 7 mmora@istituto-besta.it 2008-01-09  
  253601
LGMD2B, DYSFERLINOPATHY

58 maurizio.moggio@unimi.it 2008-06-23  
  253601
LGMD2B, DYSFERLINOPATHY
G71.0
Muscular dystrophy
18 19 19 mmora@istituto-besta.it 2008-01-09  
  253600
LGMD2A, CALPAINOPATHY
G71.0
Muscular dystrophy
18 20 20 mmora@istituto-besta.it 2008-01-09  
  253600
LGMD2A, CALPAINOPATHY

46 maurizio.moggio@unimi.it 2008-06-23  
  607801
LGMD1C, CAVEOLINOPATHY
G71.0
Muscular dystrophy
4 10 10 mmora@istituto-besta.it 2008-01-09  
  607801
LGMD1C, CAVEOLINOPATHY

60 maurizio.moggio@unimi.it 2008-06-23  
  159001
LGMD1B, LMNA
G71.0
Muscular dystrophy
6 6 6 mmora@istituto-besta.it 2008-01-09  
  253600
LGMD (UNDEFINED)
G71.0
Muscular dystrophy
33 60 34 karcagi.veronika@oki.antsz.hu 2008-07-07  
  259775
LETHAL OSTEOSCLEROTIC BONE DYSPLASIA, RAINE SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
  308000
LESCH-NYHAN SYNDROME (UNDEFINED)
E79.1
Lesch-Nyhan syndrome
2 1 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  300322
LESCH NYAN SYNDROME

1 6 3 luisa.politano@unina2.it 2008-06-30  
  151001
LENTIGINOSIS

1 1 1 saker@genethon.fr 2008-06-26  
  150800
LEIOMYOMA OF SKIN

1 8 5 saker@genethon.fr 2008-06-26  
  256000
LEIGH SYNDROME

3 6 3 saker@genethon.fr 2008-06-26  
  535000
LEBER OPTIC ATROPHY

14 54 21 saker@genethon.fr 2008-06-26  
  204000
LEBER CONGENITAL AMAUROSIS
H35.5
Leber's Congenital Amaurosis
1 1 1 mposada@isciii.es 2008-05-30  
  535000
LEBER

37 maurizio.moggio@unimi.it 2008-06-23  
  245800
LAURENCE-MOON SYNDROME

5 13 5 saker@genethon.fr 2008-06-26  
  262500
LARON SYNDROME

30 93 41 saker@genethon.fr 2008-06-26  
  604856
LANGERHANS CELL HISTIOCYTOSIS

98 102 98 saker@genethon.fr 2008-06-26  
  150230
LANGER-GIEDION SYNDROME

1 4 1 saker@genethon.fr 2008-06-26  
  159001
LAMINOPATHY; LMNA
G71.0
16 16 marina.fanin@unipd.it 2008-07-04  
  604777
LAMELLAR ICHTHYOSIS TYPE 3

1 2 1 saker@genethon.fr 2008-06-26  
  253400
KUGELBERG-WELANDER;SMA3

18 18 marina.fanin@unipd.it 2008-07-04  
  267750
KNOBLOCH SYNDROME
H54.0
Blidness, both eyes
1 9 2 karcagi.veronika@oki.antsz.hu 2008-07-07  
  173650
KINDLER SYNDROME

7 27 10 saker@genethon.fr 2008-06-26  
  245150
KEUTEL SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
  148600
KERATOSIS PALMOPLANTARIS PAPULOSA

2 4 3 saker@genethon.fr 2008-06-26  
  601952
KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA

1 9 1 saker@genethon.fr 2008-06-26  
  308800
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS

1 7 2 saker@genethon.fr 2008-06-26  
  148210
KERATITIS ICHTHYOSIS DEAFNESS SYNDROME

2 9 2 saker@genethon.fr 2008-06-26  
  313200
KENNEDY DISEASE; SBMA

15 15 marina.fanin@unipd.it 2008-07-04  
  148000
KAPOSI SARCOMA

2 2 2 saker@genethon.fr 2008-06-26  
  148000
KAPOSI SARCOMA

1 1 1 luisa.politano@unina2.it 2008-06-30  
  244200
KALLMANN SYNDROME 3

1 4 2 saker@genethon.fr 2008-06-26  
  606904
JUVENILE MYOCLONIC EPILEPSY

92 513 200 saker@genethon.fr 2008-06-26  
  213300
JOUBERT SYNDROME

3 10 4 saker@genethon.fr 2008-06-26  
  204500
JANSKY-BIELSCHOWSKY DISEASE

5 22 5 saker@genethon.fr 2008-06-26  
  600546
INTRAUTERINE GROWTH RETARDATION- SECKEL SYNDROME

3 14 4 saker@genethon.fr 2008-06-26  
  605479
INTRAEPATIC CHOLESTASIS 2

1 1 1 luisa.politano@unina2.it 2008-07-07  
  243180
INTESTINAL PSEUDOOBSTRUCTION DISEASE

18 56 19 saker@genethon.fr 2008-06-26  
  308370
INFERTILE MALE SYNDROME

2 2 2 saker@genethon.fr 2008-06-26  
  308350
INFANTILE SPASM SYNDROME- WEST SYNDROME

3 12 5 saker@genethon.fr 2008-06-26  
  269920
INFANTILE SIALIC ACID STORAGE DISORDER

1 3 1 saker@genethon.fr 2008-06-26  
  147421
INCLUSION BODY MYOSITIS

56 112 64 saker@genethon.fr 2008-06-26  
 
INCLUSION BODY MYOSITIS
G72.4
Inflammatory myopathy, not elsewhere classified
32 32 32 mmora@istituto-besta.it 2008-01-09  
  308100
ICHTHYOSIS X-LINKED

12 50 20 saker@genethon.fr 2008-06-26  
  146700
ICHTHYOSIS VULGARIS

2 8 2 saker@genethon.fr 2008-06-26  
  146700
ICHTHYOSIS VULGARIS
Q80.0
Ichthyosis vulgaris
1 2 2 mposada@isciii.es 2008-05-30  
  242300
ICHTHYOSIS LAMELLAR 1, COLLODION BABY

218 1113 313 saker@genethon.fr 2008-06-26  
  146750
ICHTHYOSIS LAMELLAR , AUTOSOMAL DOMINANT FORM

3 15 11 saker@genethon.fr 2008-06-26  
  146590
ICHTHYOSIS HYSTRIX, CURTH-MACKLIN TYPE

3 22 9 saker@genethon.fr 2008-06-26  
  308205
ICHTHYOSIS FOLLICULARIS ATRICHIA AND PHOTOPHOBIA SYNDROME

1 4 2 saker@genethon.fr 2008-06-26  
  242500
ICHTHYOSIS CONGENITA HARLEQUIN FETUS TYPE

3 12 3 saker@genethon.fr 2008-06-26  
  146800
ICHTHYOSIS BULLOUS TYPE

1 3 1 saker@genethon.fr 2008-06-26  
  242100
ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL, NONBULLOUS
Q 80
Congenital ichthyosis
2 4 4 mposada@isciii.es 2008-05-30  
  146800
ICHTHYOSIFORM ERYTHRODERMA, BULLOUS
Q80.3
Congenital bullous ichthyosiform erythroderma
3 4 4 mposada@isciii.es 2008-05-30  
 
IBM

8 maurizio.moggio@unimi.it 2008-06-23  
  307800
HYPOPHOSPHATEMIA X-LINKED

10 21 11 saker@genethon.fr 2008-06-26  
  170400
HYPOKALIEMIC PERIODIC PARALYSIS
G72.3
Periodic paralysis
11 12 12 mmora@istituto-besta.it 2008-01-09  
  170400
HYPOKALEMIC PERIODIC PARALYSIS

9 15 12 saker@genethon.fr 2008-06-26  
  202400
HYPOFIBRINOGENEMIA, CONGENITAL, INCLUDED
D 68.8
Hypofibrinogenemia
1 1 1 mposada@isciii.es 2008-05-30  
  240400
HYPOASCORBEMIA

1 1 1 saker@genethon.fr 2008-06-26  
  154850
HYPERTROPHY OF MASTICATORY MUSCLES

1 1 1 saker@genethon.fr 2008-06-26  
  145900
HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS

145 430 197 saker@genethon.fr 2008-06-26  
  192600
HYPERTROPHIC CARDIOMYOPATHY

20 29 20 luisa.politano@unina2.it 2008-06-30  
  170500
HYPERKALEMIC PERIODIC PARALYSIS

2 2 2 saker@genethon.fr 2008-06-26  
  607685
HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC; HES

Hypereosinophilic syndrome
1 1 1 mposada@isciii.es 2008-05-30  
  176670
HUTCHINSON-GILFORD PROGERIA

2 2 2 saker@genethon.fr 2008-06-26  
  607014
HURLER SYNDROME

1 2 1 saker@genethon.fr 2008-06-26  
  143100
HUNTINGTON DISEASE; HD
G 10
Huntington?s Disease
2 2 2 mposada@isciii.es 2008-05-30  
  143100
HUNTINGTON DISEASE; HD

13 14 14 edith.said@um.edu.mt 2008-08-27  
  143100
HUNTINGTON DISEASE (UNDEFINED)
G10
Huntingon?s disease
5 7 5 karcagi.veronika@oki.antsz.hu 2008-07-07  
  143100
HUNTINGTON DISEASE

14 16 14 saker@genethon.fr 2008-06-26  
  309900
HUNTER SYNDROME

2 5 3 saker@genethon.fr 2008-06-26  
  236200
HOMOCYSTINURIA

7 19 10 saker@genethon.fr 2008-06-26  
  162500
HNPP

1 1 marina.fanin@unipd.it 2008-07-04  
 
HIDROSADENITIS CHRONIC
L 73.2
Hidrosadenitis chronic
1 1 1 mposada@isciii.es 2008-05-30  
 
HEREDITARY SPASTIC PARAPLEGIA
G 11.4
Hereditary spastic paraplegia
10 49 38 mposada@isciii.es 2008-05-30  
  601097
HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSY; HNPP

1 2 2 edith.said@um.edu.mt 2008-08-27  
  141900
HEMOGLOBIN--BETA LOCUS; HBB

22 70 28 edith.said@um.edu.mt 2008-08-27  
  175700
GREIG SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
  305600
GOLTZ SYNDROME

2 7 3 saker@genethon.fr 2008-06-26  
  232500
GLYCOGENOSIS TYPE X

3 maurizio.moggio@unimi.it 2008-06-23  
  232600
GLYCOGENOSIS TYPE V, MC ARDLE
G74.0
Glycogen storage disease
21 21 21 mmora@istituto-besta.it 2008-01-09  
  232500
GLYCOGENOSIS TYPE IV
G74.0
Glycogen storage disease
3 3 3 mmora@istituto-besta.it 2008-01-09  
  232400
GLYCOGENOSIS TYPE III
G74.0
Glycogen storage disease
1 1 1 mmora@istituto-besta.it 2008-01-09  
  232400
GLYCOGENOSIS TYPE III

45 maurizio.moggio@unimi.it 2008-06-23  
  300257
GLYCOGENOSIS TYPE IIB, DANON
G74.0
Glycogen storage disease
1 2 2 mmora@istituto-besta.it 2008-01-09  
  232300
GLYCOGENOSIS TYPE II, POMPE
G74.0
Glycogen storage disease
34 34 34 mmora@istituto-besta.it 2008-01-09  
  232300
GLYCOGENOSIS TYPE II, POMPE

3 maurizio.moggio@unimi.it 2008-06-23  
  232300
GLYCOGENOSIS TYPE II

57 57 marina.fanin@unipd.it 2008-07-04  
  232600
GLYCOGEN STORAGE DISEASE V

103 122 104 saker@genethon.fr 2008-06-26  
  232400
GLYCOGEN STORAGE DISEASE III

1 1 1 saker@genethon.fr 2008-06-26  
  300257
GLYCOGEN STORAGE DISEASE IIB

1 1 1 saker@genethon.fr 2008-06-26  
  232300
GLYCOGEN STORAGE DISEASE II

2 3 3 saker@genethon.fr 2008-06-26  
  232300
GLYCOGEN STORAGE DISEASE II
E74.0
Glycogen storage disease (Type II)
3 9 3 luisa.politano@unina2.it 2008-06-30  
  231670
GLUTARIC ACIDAEMIA I

1 1 3 edith.said@um.edu.mt 2008-08-27  
  137580
GILLES DE LA TOURETTE SYNDROME; GTS
F 95.2
Tourette Syndrome
1 1 1 mposada@isciii.es 2008-05-30  
  256850
GIANT AXONAL NEUROPATHY 1

11 30 19 saker@genethon.fr 2008-06-26  
  231070
GERODERMA OSTEODYSPLASTICA

1 5 1 saker@genethon.fr 2008-06-26  
  604233
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES

2 2 1 saker@genethon.fr 2008-06-26  
  231000
GAUCHER DISEASE, TYPE III
E 75.2
Gaucher, disease
3 3 3 mposada@isciii.es 2008-05-30  
  230500
GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I

8 15 2 edith.said@um.edu.mt 2008-08-27  
  253700
GAMMA-SARCOGLYCANOPATHY; LGMD2C
G71.0
30 30 marina.fanin@unipd.it 2008-07-04  
  193700
FRREMAN SHELDOM SYNDROME

1 3 1 luisa.politano@unina2.it 2008-06-30  
  229300
FRIEDRICH ATAXIA
G11.1
Early-onset cerebellar ataxia
3 3 3 mmora@istituto-besta.it 2008-01-09  
  229300
FRIEDREICH ATAXIA; FXA

7 7 marina.fanin@unipd.it 2008-07-04  
  229300
FRIEDREICH ATAXIA 1, FRDA
G 11.1
Cerebellar ataxia, Friedreich
17 17 17 mposada@isciii.es 2008-05-30  
  229300
FRIEDREICH ATAXIA 1

41 147 49 saker@genethon.fr 2008-06-26  
  229300
FRIEDREICH ATAXIA (UNDEFINED)
G11.1
Early-onset cerebellar ataxia
4 5 5 karcagi.veronika@oki.antsz.hu 2008-07-07  
  229300
FRIEDREICH ATAXIA

4 8 4 luisa.politano@unina2.it 2008-06-30  
  193700
FREEMAN-SHELDON SYNDROME

1 4 1 saker@genethon.fr 2008-06-26  
  309550
FRAGILE X SYNDROME

10 19 10 saker@genethon.fr 2008-06-26  
  309550
FRAGILE SITE MENTAL RETARDATION 1 GENE; FMR1 (UNDEFINED)
Q99.2
Fragile X chromosome
180 263 169 karcagi.veronika@oki.antsz.hu 2008-07-07  
  309550
FRAGILE SITE MENTAL RETARDATION 1 GENE; FMR1 (DEFINED)
Q99.2
Fragile X chromosome
35 64 38 karcagi.veronika@oki.antsz.hu 2008-07-07  
  256300
FINNISH NEPHROTIC SYNDROME

1 1 3 edith.said@um.edu.mt 2008-08-27  
  135100
FIBRODYSPLASIA OSSIFICANS PROGRESSIVA

8 18 9 saker@genethon.fr 2008-06-26  
 
FIBER TYPE DISPROPORTION
G71.2
Congenital myopathies
17 17 17 mmora@istituto-besta.it 2008-01-09  
  305450
FG SYNDROME

2 5 2 saker@genethon.fr 2008-06-26  
  153640
FECHTENER SYNDROME

1 4 1 luisa.politano@unina2.it 2008-06-30  
  121210
FEBRILE CONVULSIONS FAMILIAL

109 797 390 saker@genethon.fr 2008-06-26  
  227810
FANCONI-BICKEL SYNDROME

3 3 3 saker@genethon.fr 2008-06-26  
  227650
FANCONI ANEMIA

60 262 66 saker@genethon.fr 2008-06-26  
  601606
FAMILIAL TRICHOEPITHELIOMATA

1 2 2 edith.said@um.edu.mt 2008-08-27  
  249100
FAMILIAL MEDITERRANEAN FEVER; FMF

10 19 9 edith.said@um.edu.mt 2008-08-27  
  249100
FAMILIAL MEDITERRANEAN FEVER

149 607 233 saker@genethon.fr 2008-06-26  
  160750
FAMILIAL IDIOPATHIC INFLAMMATORY MYOPATHY

1 2 1 saker@genethon.fr 2008-06-26  
  158900
FACIO-SCAPULO-HUMERAL;FSHD1A
G71.0
63 63 marina.fanin@unipd.it 2008-07-04  
  158900
FACIO-SCAPULO-HUMERAL, FSHD1
G71.0
Muscular dystrophy
50 118 100 mmora@istituto-besta.it 2008-01-09  
  158900
FACIO-SCAPULO-HUMERAL MUSCULAR DYSTROPHY; FSHD1

4 4 4 edith.said@um.edu.mt 2008-08-27  
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A (UNDEFINED)
G71.0
Muscular dystrophy
53 110 43 karcagi.veronika@oki.antsz.hu 2008-07-07  
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A (DEFINED)
G71.0
Muscular dystrophy
53 80 80 karcagi.veronika@oki.antsz.hu 2008-07-07  
  158900
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A
G71.0
Muscular dystrophy
109 163 163 luisa.politano@unina2.it 2008-06-30  
  158900
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY

258 709 358 saker@genethon.fr 2008-06-26  
  133450
EWING SARCOMA

1 1 1 saker@genethon.fr 2008-06-26  
 
ESSENTIAL HYPERCKEMIA

10 maurizio.moggio@unimi.it 2008-06-23  
  265000
ESCOBAR SYNDROME

1 6 2 saker@genethon.fr 2008-06-26  
  133200
ERYTHROKERATODERMIA VARIABILIS

2 11 2 saker@genethon.fr 2008-06-26  
  602036
ERYTHROKERATODERMIA PROGRESSIVE SYMMETRIC

4 40 14 saker@genethon.fr 2008-06-26  
  108500
EPISODIC ATAXIA
G 11.2
Late-onset cerebellar ataxia
2 2 2 mposada@isciii.es 2008-05-30  
  266100
EPILEPSY PYRIDOXINE-DEPENDENT

7 29 13 saker@genethon.fr 2008-06-26  
  254800
EPILEPSY PROGRESSIVE MYOCLONIC

23 71 36 saker@genethon.fr 2008-06-26  
  132100
EPILEPSY PHOTOGENIC

4 25 11 saker@genethon.fr 2008-06-26  
  600513
EPILEPSY NOCTURNAL FRONTAL LOBE

11 64 28 saker@genethon.fr 2008-06-26  
  607631
EPILEPSY JUVENILE ABSENCE

62 311 140 saker@genethon.fr 2008-06-26  
  600669
EPILEPSY IDIOPATHIC GENERALIZED

35 168 76 saker@genethon.fr 2008-06-26  
  132090
EPILEPSY BENIGN OCCIPITAL

2 13 6 saker@genethon.fr 2008-06-26  
  121200
EPILEPSY BENIGN NEONATAL

24 167 78 saker@genethon.fr 2008-06-26  
  601001
EPIDERMOLYSIS BULLOSA SIMPLEX

4 20 8 saker@genethon.fr 2008-06-26  
  131850
EPIDERMOLYSIS BULLOSA PRETIBIAL

1 5 3 saker@genethon.fr 2008-06-26  
  131900
EPIDERMOLYSIS BULLOSA KOBNER TYPE

3 14 5 saker@genethon.fr 2008-06-26  
  226450
EPIDERMOLYSIS BULLOSA INVERSA DYSTROPHICA

1 6 1 saker@genethon.fr 2008-06-26  
  131760
EPIDERMOLYSIS BULLOSA HERPETIFORMIS, DOWLING-MEARA TYPE

21 194 40 saker@genethon.fr 2008-06-26  
  226650
EPIDERMOLYSIS BULLOSA GENERALIZED ATROPHIC BENIGN

20 144 12 saker@genethon.fr 2008-06-26  
  131750
EPIDERMOLYSIS BULLOSA DYSTROPHICA PASINI TYPE

11 47 18 saker@genethon.fr 2008-06-26  
  226600
EPIDERMOLYSIS BULLOSA DYSTROPHICA HALLOREAU-SIEMENS TYPE

65 256 79 saker@genethon.fr 2008-06-26  
  131800
EPIDERMOLYSIS BULLOSA OF HANDS AND FEET

4 11 5 saker@genethon.fr 2008-06-26  
  226400
EPIDERMODYSPLASIA VERRUCIFORMIS

32 226 40 saker@genethon.fr 2008-06-26  
  310300
EMERY-DREIFUSS MUSCULAR DYSTROPHY,X-LINKED; EDMD1
G71.0
Muscular dystrophy (Emery-Dreifuss)
7 34 14 luisa.politano@unina2.it 2008-06-30  
  310300
EMERY-DREIFUSS MUSCULAR DYSTROPHY, X-LINKED; EDMD (UNDEFINED)
G71.0
Muscular dystrophy
4 7 4 karcagi.veronika@oki.antsz.hu 2008-07-07  
  310300
EMERY-DREIFUSS MUSCULAR DYSTROPHY, AD-LINKED; EDMD; LMNA (DEFINED)
G71.0
Muscular dystrophy
1 3 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  181350
EMERY-DREIFUS MUSCULAR DYSTROPHY

99 276 132 saker@genethon.fr 2008-06-26  
  130050
EHLERS-DANLOS SYNDROME TYPE IV

1 6 4 saker@genethon.fr 2008-06-26  
  130000
EHLERS-DANLOS SYNDROME TYPE 1

4 31 7 saker@genethon.fr 2008-06-26  
  606408
EHLERS-DANLOS LIKE SYNDROME DUE TO TENASCIN-X DEFICIENCY

1 1 1 saker@genethon.fr 2008-06-26  
  310300
EDMD X-LINKED
G71.0
Muscular dystrophy
6 6 6 mmora@istituto-besta.it 2008-01-09  
  129500
ECTODERMAL DYSPLASIA HIDROTIC

7 66 28 saker@genethon.fr 2008-06-26  
  224900
ECTODERMAL DYSPLASIA ANHIDROTIC

6 22 10 saker@genethon.fr 2008-06-26  
  160900
DYSTROPHIA MYOTONICA 1 (DEFINED)
G71.1
Myotonic disorders
25 37 33 karcagi.veronika@oki.antsz.hu 2008-07-07  
  160900
DYSTROPHIA MYOTONICA 1
G71.1
Myotonic disorders (DM1)
73 133 123 luisa.politano@unina2.it 2008-06-30  
  160900
DYSTROPHIA MYOTONICA 1
G 71.1
Steinert's Disease
1 7 7 mposada@isciii.es 2008-05-30  
  160900
DYSTROPHIA MYOTONICA (UNDEFINED)
G71.1
Myotonic disorders
27 32 26 karcagi.veronika@oki.antsz.hu 2008-07-07  
  160900
DYSTROPHIA MYOTONICA

91 153 109 saker@genethon.fr 2008-06-26  
 
DYSTONIA, TORSION (DEFINED)
G24
1 5 3 karcagi.veronika@oki.antsz.hu 2008-07-07