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Results for your request: type = DNA
635
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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  
 
G12.2
Motor neuron disease (ALS)
2 2 2 luisa.politano@unina2.it 2008-06-30  
 
G71.3
Mitochondrial myopathy, not elsewhere classified (Respiratory Chain deficiency)
6 6 6 luisa.politano@unina2.it 2008-06-30  
 
M33.2
Polymyositis
1 2 1 luisa.politano@unina2.it 2008-06-30  
 

Ichthyosis controls
16 28 mposada@isciii.es 2008-05-30  
  146750
ICHTHYOSIS, LAMELLAR
Q80.2
ICHTHYOSIS, LAMELLAR Q80.2
6 12 12 mposada@isciii.es 2008-05-30  
  253600
LGMD2A LGMD2C (DEFINED)
G71.0
Muscular dystrophy
20 51 34 karcagi.veronika@oki.antsz.hu 2008-07-07  
  200100
ABETALIPOPROTEINEMIA

1 1 1 saker@genethon.fr 2008-06-26  
  100600
ACANTHOSIS NIGRICANS

1 10 4 saker@genethon.fr 2008-06-26  
  232300
ACID MALTASE DEFICIENCY

3 8 6 luisa.politano@unina2.it 2008-06-30  
  201100
ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY

1 4 3 saker@genethon.fr 2008-06-26  
  201200
ACROGERIA

1 2 1 saker@genethon.fr 2008-06-26  
  101400
ACTH DEFICIENCY
E 27.1
ACTH deficiency
1 1 1 mposada@isciii.es 2008-05-30  
  175100
ADENOMATOUS POLYPOSIS OF THE COLON

150 172 137 saker@genethon.fr 2008-06-26  
  175100
ADENOMATOUS POLYPOSIS OF THE COLON; APC
D12.6
Polyposis (hereditery) of colon
1 1 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  103050
ADENYLOSUCCINASE DEFICIENCY

1 1 1 saker@genethon.fr 2008-06-26  
  300100
ADRENOLEUKODYSTROPHY

5 8 5 saker@genethon.fr 2008-06-26  
  300100
ADRENOLEUKODYSTROPHY; ALD (UNDEFINED)
Q98
Disorders of fatty-acid metabolism
4 7 5 karcagi.veronika@oki.antsz.hu 2008-07-07  
  225750
AICARDI-GOUTIERES SYNDROME

35 140 49 saker@genethon.fr 2008-06-26  
  300500
ALBINISM OCULAR TYPE 1

2 2 2 saker@genethon.fr 2008-06-26  
  104110
ALOPECIA FAMILIAL

1 3 3 saker@genethon.fr 2008-06-26  
  107400
ALPHA-1-ANTITRYPSIN DEFICIENCY
E 28.2
Alpha-1-antitrypsin deficit
1 1 1 mposada@isciii.es 2008-05-30  
  608099
ALPHA-SARCOGLYCANOPATHY; LGMD2D
G71.0
68 68 marina.fanin@unipd.it 2008-07-04  
  104200
ALPORT SYNDROME

176 245 209 saker@genethon.fr 2008-06-26  
 
ALS/ MOTOR NEURON DISEASE
G12.2
Motor neuron disease
72 72 72 mmora@istituto-besta.it 2008-01-09  
 
ALS/MOTOR NEURON DISEASE

81 maurizio.moggio@unimi.it 2008-06-23  
  105400
AMYOTROPHIC LATERAL SCLEROSIS

2 2 2 luisa.politano@unina2.it 2008-07-07  
  181400
AMYOTROPHY SCAPULOPERONEAL

9 20 10 saker@genethon.fr 2008-06-26  
  105830
ANGELMAN SYNDROME

6 16 8 saker@genethon.fr 2008-06-26  
  106100
ANGIOEDEMA, HEREDITARY; HAE/ANGIONEUROTIC EDEMA
D 84.1
C1-inhibidor deficiency
2 2 2 mposada@isciii.es 2008-05-30  
  106200
ANIRIDIA

1 5 1 saker@genethon.fr 2008-06-26  
  107741
APOLIPOPROTEIN E

2 2 2 saker@genethon.fr 2008-06-26  
  107970
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA FAMILIAL

6 14 5 saker@genethon.fr 2008-06-26  
  108110
ARTHROGRYPOSIS MULTIPLEX CONGENITA

17 42 16 saker@genethon.fr 2008-06-26  
  208230
ARTHROPATHY PROGRESSIVE PSEUDORHUMATOID OF CHILDHOOD

9 48 18 saker@genethon.fr 2008-06-26  
  208500
ASPHYXIATING THORACIC DYSTROPHY

1 1 1 saker@genethon.fr 2008-06-26  
  148360
AXONAL NEUROPATHY WITH PALMOPLANTAR KERATODERMA

1 2 1 saker@genethon.fr 2008-06-26  
  415000
AZF (SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED) (UNDEFINED)
Q98
Other sex chromosome abnormalities, male phenotype, not elsewhere classified
1 2 2 karcagi.veronika@oki.antsz.hu 2008-07-07  
  109400
BASAL CELL NEVUS SYNDROME

3 14 7 saker@genethon.fr 2008-06-26  
  204200
BATTEN DISEASE; UNDEFINED

1 1 1 edith.said@um.edu.mt 2008-08-27  
  301845
BAZEX SYNDROME

1 4 3 saker@genethon.fr 2008-06-26  
  109650
BECHET SYNDROME
M 35.1
Bechet's Disease
22 25 21 mposada@isciii.es 2008-05-30  
  300376
BECKER DYSTROPHY, BMD
G71.0
Muscular dystrophy
152 155 155 mmora@istituto-besta.it 2008-01-09  
  300376
BECKER DYSTROPHY, BMD

220 maurizio.moggio@unimi.it 2008-06-23  
  310100
BECKER DYSTROPHY;BMD
G71.0
31 31 marina.fanin@unipd.it 2008-07-04  
  130650
BECKWITH-WIEDEMANN SYNDROME

42 49 45 saker@genethon.fr 2008-06-26  
  117100
BENIGN ROLANDIC EPILEPSY

3 10 5 saker@genethon.fr 2008-06-26  
  604286
BETA-SARCOGLYCANOPATHY; LGMD2E
G71.0
24 24 marina.fanin@unipd.it 2008-07-04  
  120220
BETHLEM MYOPATHY
G71.2
Congenital myopathy (Bethlem myopathy)
3 7 6 luisa.politano@unina2.it 2008-06-30  
  210900
BLOOM SYNDROME

1 3 1 saker@genethon.fr 2008-06-26  
  310100
BMD CARRIER

3 3 marina.fanin@unipd.it 2008-07-04  
  162100
BRACHIAL PLEXUS NEUROPATHY, HEREDITARY AMYOTROPHY

1 1 1 saker@genethon.fr 2008-06-26  
  113620
BRANCHIAL CLEFTS WITH CHARACTERISTIC FACIES

1 1 1 saker@genethon.fr 2008-06-26  
  601003
BRODY MYOPATHY

4 6 6 saker@genethon.fr 2008-06-26  
  601144
BRUGADA SYNDROME

5 34 7 luisa.politano@unina2.it 2008-06-30  
  211500
BULBAR PALSY PROGRESSIVE OF CHILDHOOD

1 1 1 saker@genethon.fr 2008-06-26  
  114140
CALLOSITIES HEREDITARY PAINFUL

1 2 2 saker@genethon.fr 2008-06-26  
  253600
CALPAINOPATHY;LGMD2A
G71.0
199 199 marina.fanin@unipd.it 2008-07-04  
  271900
CANAVAN DISEASE

2 9 2 saker@genethon.fr 2008-06-26  
  115200
CARDIOMYOPATHY DILATED

185 671 277 saker@genethon.fr 2008-06-26  
  192600
CARDIOMYOPATHY FAMILIAL HYPERTROPHIC

266 1340 62 saker@genethon.fr 2008-06-26  
  212160
CARNITINE DEFICIENCY

1 1 1 luisa.politano@unina2.it 2008-06-30  
  607801
CAVEOLINOPATHY;LGMD1C
G71.0
15 15 marina.fanin@unipd.it 2008-07-04  
  117000
CENTRAL CORE DISEASE OF MUSCLE

113 523 197 saker@genethon.fr 2008-06-26  
  117000
CENTRALCORE MYOPATHY
G71.2
Congenital myopathies (Central core disease)
9 9 9 luisa.politano@unina2.it 2008-06-30  
 
CENTRALCORE MYOPATHY
G71.2
Congenital myopathies
16 16 16 mmora@istituto-besta.it 2008-01-09  
  255200
CENTRONUCLEAR MYOPATHY

63 226 95 saker@genethon.fr 2008-06-26  
 
CENTRONUCLEAR MYOPATHY
G71.2
Congenital myopathies
18 18 18 mmora@istituto-besta.it 2008-01-09  
  212800
CEREBELLAR ATAXIA

1 1 1 luisa.politano@unina2.it 2008-06-30  
  117360
CEREBELLAR ATAXIA

2 15 3 saker@genethon.fr 2008-06-26  
  212840
CEREBELLAR ATAXIA
G 11.3
Cerebellar ataxia
8 11 11 mposada@isciii.es 2008-05-30  
  302500
CEREBELLAR ATAXIA 2

3 13 4 saker@genethon.fr 2008-06-26  
  117210
CEREBELLAR ATAXIA, AUTOSOMAL DOMINANT

12 29 22 saker@genethon.fr 2008-06-26  
  125310
CEREBRAL ARTERIOPATHY, AUTOSOMAL DOMINANT; CADASIL (UNDEFINED)

Progressive vascular leukoencephalopathy
2 2 2 karcagi.veronika@oki.antsz.hu 2008-07-07  
  256730
CEROID LIPOFUSCINOSIS (UNDEFINED) CLN1, CLN2, CLN3, CLN4, CLN5, CLN6, CLN7, CLN8, CLN9
E75.4
Neuronal ceroid lipofuscinosis
3 6 3 karcagi.veronika@oki.antsz.hu 2008-07-07  
  204500
CEROID LIPOFUSCINOSIS CLN2 (DEFINED)
E75.4
Neuronal ceroid lipofuscinosis
2 5 2 karcagi.veronika@oki.antsz.hu 2008-07-07  
  256730
CEROID LIPOFUSCINOSIS NEURONAL 1

3 9 3 saker@genethon.fr 2008-06-26  
  170400
CHANNELLOPATHIES

4 13 4 luisa.politano@unina2.it 2008-06-30  
  118200
CHARCOT MARIE-TOOTH

1 1 1 edith.said@um.edu.mt 2008-08-27  
  118220
CHARCOT MARIE-TOOTH; HMSN1A DEFINED

1 1 1 edith.said@um.edu.mt 2008-08-27  
  118220
CHARCOT-MARIE-TOOTH DISEASE (UNDEFINED)
G60.0
Hereditary motor and sensory neuropathy
115 197 117 karcagi.veronika@oki.antsz.hu 2008-07-07  
  118210
CHARCOT-MARIE-TOOTH DISEASE AXONAL TYPE 2A

34 81 40 saker@genethon.fr 2008-06-26  
  118200
CHARCOT-MARIE-TOOTH DISEASE DEMYELINATING TYPE 1B

18 54 26 saker@genethon.fr 2008-06-26  
  214400
CHARCOT-MARIE-TOOTH DISEASE TYPE 4A

7 20 13 saker@genethon.fr 2008-06-26  
  118220
CHARCOT-MARIE-TOOTH DISEASE, CMT1A (DEFINED)
G60.0
Hereditary motor and sensory neuropathy
35 83 63 karcagi.veronika@oki.antsz.hu 2008-07-07  
  118220
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A; CMT1A
G 60.0
Charcot-Marie-Tooth Disease
1 2 2 mposada@isciii.es 2008-05-30  
  118200
CHARCOT-MARIE-TOOTH; CMT

4 7 7 luisa.politano@unina2.it 2008-06-30  
  302045
CHARCOT-MARIE-TOOTH; CMT + DEAFNESS

2 5 5 luisa.politano@unina2.it 2008-06-30  
  214500
CHEDIAK-HIGASHI SYNDROME

2 7 3 saker@genethon.fr 2008-06-26  
  118400
CHERUBISM

2 11 4 saker@genethon.fr 2008-06-26  
  118600
CHONDROCALCINOSIS 2

10 38 9 saker@genethon.fr 2008-06-26  
  303100
CHOROIDEREMIA

3 3 3 saker@genethon.fr 2008-06-26  
 
CHRONIC FATIGUE SYNDROME
G 93.3
Chronic Fatigue Syndrome
1 1 1 mposada@isciii.es 2008-05-30  
  606612
CMD, MUSCULAR DYSTROPHY, CONGENITAL (UNDEFINED)
G71.2
Congenital myopathies
5 5 5 karcagi.veronika@oki.antsz.hu 2008-07-07  
  608931
CMS - MYASTHENIC SYNDROME, CONGENITAL, WITH FACIAL DYSMORPHISM, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY, INCLUDED (DEFINED)
G70.2
Congenital and developmental myasthenia
47 169 69 karcagi.veronika@oki.antsz.hu 2008-07-07  
  608931
CMS - MYASTHENIC SYNDROME, CONGENITAL, WITH FACIAL DYSMORPHISM, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY, INCLUDED (UNDEFINED)
G70.2
Congenital and developmental myasthenia
37 76 39 karcagi.veronika@oki.antsz.hu 2008-07-07  
 
CMT LOM (DEFINED)
G60.0
Hereditary motor and sensory neuropathy
3 14 3 karcagi.veronika@oki.antsz.hu 2008-07-07  
  216400
COCKAYNE SUNDROME

7 13 6 saker@genethon.fr 2008-06-26  
  216550
COHEN SYNDROME

3 5 2 saker@genethon.fr 2008-06-26  
  120435
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 1; HNPCC1

1 1 1 edith.said@um.edu.mt 2008-08-27  
  120970
CONE-ROD DYSTROPHY 2

46 227 84 saker@genethon.fr 2008-06-26  
  304020
CONE-ROD DYSTROPHY, X-LINKED

21 77 30 saker@genethon.fr 2008-06-26  
 
CONGENITAL DYSTROPHIES

9 maurizio.moggio@unimi.it 2008-06-23  
  606612
CONGENITAL DYSTROPHY. FKRP
G71.2
Congenital myopathies
4 4 4 mmora@istituto-besta.it 2008-01-09  
  606822
CONGENITAL DYSTROPHY. POMGNT1
G71.2
Congenital myopathies
1 1 1 mmora@istituto-besta.it 2008-01-09  
  607423
CONGENITAL DYSTROPHY. POMT1
G71.2
Congenital myopathies
4 4 4 mmora@istituto-besta.it 2008-01-09  
  607439
CONGENITAL DYSTROPHY. POMT2
G71.2
Congenital myopathies
2 2 2 mmora@istituto-besta.it 2008-01-09  
  263700
CONGENITAL ERYTHROPOIETIC PORPHYRIA

3 3 3 saker@genethon.fr 2008-06-26  
  242100
CONGENITAL ICHTHYOSIFORM ERYTHRODERMA

25 80 32 saker@genethon.fr 2008-06-26  
  253800
CONGENITAL MUSCULAR DYSTROPHY

429 1292 461 saker@genethon.fr 2008-06-26  
 
CONGENITAL MYASTENIA
G70.2
Congenital and developmental myasthenia
3 3 3 mmora@istituto-besta.it 2008-01-09  
  254210
CONGENITAL MYASTENIA

1 1 1 luisa.politano@unina2.it 2008-07-07  
  601462
CONGENITAL MYASTHENIC SYNDROME

171 443 221 saker@genethon.fr 2008-06-26  
  168300
CONGENITAL PARAMYOTONIA SCN4A
G71.1
Myotonic disorders
1 3 3 mmora@istituto-besta.it 2008-01-09  
 
CONNECTIVITIS
M35
Other systemic involvement of connective tissue
12 12 12 mmora@istituto-besta.it 2008-01-09  
 
CONTROL

Control
525 mposada@isciii.es 2008-05-30  
 
CONTROL

450 450 luisa.politano@unina2.it 2008-07-07  
 
CONTROL SAMPLES

440 luisa.politano@unina2.it 2008-06-30  
 
CONTROLS

320 320 320 mmora@istituto-besta.it 2008-01-09  
 
CONTROLS

1000 1000 1000 edith.said@um.edu.mt 2008-08-27  
  601764
CONVULSIONS BENIGN FAMILIAL INFANTILE

21 158 70 saker@genethon.fr 2008-06-26  
  217200
CONVULSIVE DISORDER WITH ORENATAL OR EARLY ONSET

1 4 saker@genethon.fr 2008-06-26  
  218040
COSTELLO SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
  220110
COX DEFECT

7 7 marina.fanin@unipd.it 2008-07-04  
  530000
CPEO KEARNS-SAYRE SYNDROME (DEFINED)
H49.8
Other paralytic strabismus
1 1 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  530000
CPEO KEARNS-SAYRE SYNDROME (UNDEFINED)
H49.8
Other paralytic strabismus
2 2 2 karcagi.veronika@oki.antsz.hu 2008-07-07  
  255110
CPT DEFICIENCY

35 maurizio.moggio@unimi.it 2008-06-23  
  255110
CPT DEFICIENCY

5 5 marina.fanin@unipd.it 2008-07-04  
  255110
CPT DEFICIENCY
E71.3
Disorders of fatty-acid metabolism
25 25 25 mmora@istituto-besta.it 2008-01-09  
  123500
CROUZON SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
  123700
CUTIS-LAXA

28 107 41 saker@genethon.fr 2008-06-26  
  219700
CYSTIC FIBROSIS

3 9 6 saker@genethon.fr 2008-06-26  
  219700
CYSTIC FIBROSIS; CF
E 84
Fibrosis quistic
5 5 5 mposada@isciii.es 2008-05-30  
  219700
CYSTIC FIBROSIS; CF

1 1 1 edith.said@um.edu.mt 2008-08-27  
  220200
DANDY-WALKER SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
  300257
DANON DISEASE; LAMP2

16 16 marina.fanin@unipd.it 2008-07-04  
  601287
DELTA-SARCOGLYCANOPATHY; LGMD2F
G71.0
4 4 marina.fanin@unipd.it 2008-07-04  
 
DERMATOMYOSITIS
M33
Dermatopolymyositis
46 46 46 mmora@istituto-besta.it 2008-01-09  
  135290
DESMOID DISEASE

12 12 12 saker@genethon.fr 2008-06-26  
  222100
DIABETES MELLITUS INSULIN-DEPENDENT

72 431 205 saker@genethon.fr 2008-06-26  
  125853
DIABETES MELLITUS NONINSULIN-DEPENDENT

127 248 14 saker@genethon.fr 2008-06-26  
  105650
DIAMOND-BLACKFAN ANEMIA

99 373 110 saker@genethon.fr 2008-06-26  
  188400
DIGEORGE SYNDROME

18 37 18 saker@genethon.fr 2008-06-26  
  115200
DILATED CARDIOMYOPATHIES

15 15 15 luisa.politano@unina2.it 2008-06-30  
 
DISENDOCRINE MYOPATHY
G73.5*
Myopathy in endocrine diseases
8 8 8 mmora@istituto-besta.it 2008-01-09  
  253601
DISFERLINOPATHY;LGMD2B
G71.0
58 58 marina.fanin@unipd.it 2008-07-04  
 
DISTAL MYOPATHY
G71.0
Muscular dystrophy
2 2 2 mmora@istituto-besta.it 2008-01-09  
  310200
DMD CARRIER

13 13 marina.fanin@unipd.it 2008-07-04  
  310200
DMD/BMD CARRIER

9 maurizio.moggio@unimi.it 2008-06-23  
  310200
DMD/BMD CARRIER
G71.0
Muscular dystrophy
62 65 65 mmora@istituto-besta.it 2008-01-09  
  310200
DMD/BMD CARRIERS
G71.0
Muscular dystrophy (Carrier of MD Duchenne/Becker)
623 1397 379 luisa.politano@unina2.it 2008-06-30  
  300121
DOUBLECORTIN

23 106 23 saker@genethon.fr 2008-06-26  
  190685
DOWN?S SYNDROME (UNDEFINED)
Q90.9
Down syndrome
1 3 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  126600
DRUSEN RADIAL AUTOSOMAL DOMINANT

1 2 saker@genethon.fr 2008-06-26  
  310200
DUCHENNE DYSTROPHY, DMD

208 maurizio.moggio@unimi.it 2008-06-23  
  310200
DUCHENNE DYSTROPHY, DMD
G71.0
Muscular dystrophy
141 142 142 mmora@istituto-besta.it 2008-01-09  
  310200
DUCHENNE DYSTROPHY;DMD
G71.0
76 76 marina.fanin@unipd.it 2008-07-04  
  310200
DUCHENNE MUSCULAR DYSTROPHY; DMD

6 6 6 edith.said@um.edu.mt 2008-08-27  
  310200
DUCHENNE/BECKER DYSTROPHY
G71.0
6 6 marina.fanin@unipd.it 2008-07-04  
  310200
DUCHENNE/BECKER MUSCULAR DYSTROPHY (DEFINED)
G71.1
Muscular dystrophy
105 156 111 karcagi.veronika@oki.antsz.hu 2008-07-07  
  310200
DUCHENNE/BECKER MUSCULAR DYSTROPHY(UNDEFINED)
G71.1
Muscular dystrophy
67 122 54 karcagi.veronika@oki.antsz.hu 2008-07-07  
  600117
DYSPHASIA FAMILIAL DEVELOPMENTAL

4 14 13 saker@genethon.fr 2008-06-26  
  128230
DYSTONIA PROGRESSIVE WITH DIURNAL VARIATION

9 19 5 saker@genethon.fr 2008-06-26  
 
DYSTONIA, TORSION ( UNDEFINED)
G24
3 15 3 karcagi.veronika@oki.antsz.hu 2008-07-07  
 
DYSTONIA, TORSION (DEFINED)
G24
1 5 3 karcagi.veronika@oki.antsz.hu 2008-07-07  
  160900
DYSTROPHIA MYOTONICA

91 153 109 saker@genethon.fr 2008-06-26  
  160900
DYSTROPHIA MYOTONICA (UNDEFINED)
G71.1
Myotonic disorders
27 32 26 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 1 (DEFINED)
G71.1
Myotonic disorders
25 37 33 karcagi.veronika@oki.antsz.hu 2008-07-07  
  224900
ECTODERMAL DYSPLASIA ANHIDROTIC

6 22 10 saker@genethon.fr 2008-06-26  
  129500
ECTODERMAL DYSPLASIA HIDROTIC

7 66 28 saker@genethon.fr 2008-06-26  
  310300
EDMD X-LINKED
G71.0
Muscular dystrophy
6 6 6 mmora@istituto-besta.it 2008-01-09  
  606408
EHLERS-DANLOS LIKE SYNDROME DUE TO TENASCIN-X DEFICIENCY

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

4 31 7 saker@genethon.fr 2008-06-26  
  130050
EHLERS-DANLOS SYNDROME TYPE IV

1 6 4 saker@genethon.fr 2008-06-26  
  181350
EMERY-DREIFUS MUSCULAR DYSTROPHY

99 276 132 saker@genethon.fr 2008-06-26  
  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  
  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,X-LINKED; EDMD1
G71.0
Muscular dystrophy (Emery-Dreifuss)
7 34 14 luisa.politano@unina2.it 2008-06-30  
  226400
EPIDERMODYSPLASIA VERRUCIFORMIS

32 226 40 saker@genethon.fr 2008-06-26  
  131800
EPIDERMOLYSIS BULLOSA OF HANDS AND FEET

4 11 5 saker@genethon.fr 2008-06-26  
  226600
EPIDERMOLYSIS BULLOSA DYSTROPHICA HALLOREAU-SIEMENS TYPE

65 256 79 saker@genethon.fr 2008-06-26  
  131750
EPIDERMOLYSIS BULLOSA DYSTROPHICA PASINI TYPE

11 47 18 saker@genethon.fr 2008-06-26  
  226650
EPIDERMOLYSIS BULLOSA GENERALIZED ATROPHIC BENIGN

20 144 12 saker@genethon.fr 2008-06-26  
  131760
EPIDERMOLYSIS BULLOSA HERPETIFORMIS, DOWLING-MEARA TYPE

21 194 40 saker@genethon.fr 2008-06-26  
  226450
EPIDERMOLYSIS BULLOSA INVERSA DYSTROPHICA

1 6 1 saker@genethon.fr 2008-06-26  
  131900
EPIDERMOLYSIS BULLOSA KOBNER TYPE

3 14 5 saker@genethon.fr 2008-06-26  
  131850
EPIDERMOLYSIS BULLOSA PRETIBIAL

1 5 3 saker@genethon.fr 2008-06-26  
  601001
EPIDERMOLYSIS BULLOSA SIMPLEX

4 20 8 saker@genethon.fr 2008-06-26  
  121200
EPILEPSY BENIGN NEONATAL

24 167 78 saker@genethon.fr 2008-06-26  
  132090
EPILEPSY BENIGN OCCIPITAL

2 13 6 saker@genethon.fr 2008-06-26  
  600669
EPILEPSY IDIOPATHIC GENERALIZED

35 168 76 saker@genethon.fr 2008-06-26  
  607631
EPILEPSY JUVENILE ABSENCE

62 311 140 saker@genethon.fr 2008-06-26  
  600513
EPILEPSY NOCTURNAL FRONTAL LOBE

11 64 28 saker@genethon.fr 2008-06-26  
  132100
EPILEPSY PHOTOGENIC

4 25 11 saker@genethon.fr 2008-06-26  
  254800
EPILEPSY PROGRESSIVE MYOCLONIC

23 71 36 saker@genethon.fr 2008-06-26  
  266100
EPILEPSY PYRIDOXINE-DEPENDENT

7 29 13 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  
  602036
ERYTHROKERATODERMIA PROGRESSIVE SYMMETRIC

4 40 14 saker@genethon.fr 2008-06-26  
  133200
ERYTHROKERATODERMIA VARIABILIS

2 11 2 saker@genethon.fr 2008-06-26  
  265000
ESCOBAR SYNDROME

1 6 2 saker@genethon.fr 2008-06-26  
 
ESSENTIAL HYPERCKEMIA

10 maurizio.moggio@unimi.it 2008-06-23  
  133450
EWING SARCOMA

1 1 1 saker@genethon.fr 2008-06-26  
  158900
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY

258 709 358 saker@genethon.fr 2008-06-26  
  158900
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A
G71.0
Muscular dystrophy
109 163 163 luisa.politano@unina2.it 2008-06-30  
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A (DEFINED)
G71.0
Muscular dystrophy
53 80 80 karcagi.veronika@oki.antsz.hu 2008-07-07  
 
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A (UNDEFINED)
G71.0
Muscular dystrophy
53 110 43 karcagi.veronika@oki.antsz.hu 2008-07-07  
  158900
FACIO-SCAPULO-HUMERAL MUSCULAR DYSTROPHY; FSHD1

4 4 4 edith.said@um.edu.mt 2008-08-27  
  158900
FACIO-SCAPULO-HUMERAL, FSHD1
G71.0
Muscular dystrophy
50 118 100 mmora@istituto-besta.it 2008-01-09  
  158900
FACIO-SCAPULO-HUMERAL;FSHD1A
G71.0
63 63 marina.fanin@unipd.it 2008-07-04  
  160750
FAMILIAL IDIOPATHIC INFLAMMATORY MYOPATHY

1 2 1 saker@genethon.fr 2008-06-26  
  249100
FAMILIAL MEDITERRANEAN FEVER

149 607 233 saker@genethon.fr 2008-06-26  
  249100
FAMILIAL MEDITERRANEAN FEVER; FMF

10 19 9 edith.said@um.edu.mt 2008-08-27  
  601606
FAMILIAL TRICHOEPITHELIOMATA

1 2 2 edith.said@um.edu.mt 2008-08-27  
  227650
FANCONI ANEMIA

60 262 66 saker@genethon.fr 2008-06-26  
  227810
FANCONI-BICKEL SYNDROME

3 3 3 saker@genethon.fr 2008-06-26  
  121210
FEBRILE CONVULSIONS FAMILIAL

109 797 390 saker@genethon.fr 2008-06-26  
  153640
FECHTENER SYNDROME

1 4 1 luisa.politano@unina2.it 2008-06-30  
  305450
FG SYNDROME

2 5 2 saker@genethon.fr 2008-06-26  
 
FIBER TYPE DISPROPORTION
G71.2
Congenital myopathies
17 17 17 mmora@istituto-besta.it 2008-01-09  
  135100
FIBRODYSPLASIA OSSIFICANS PROGRESSIVA

8 18 9 saker@genethon.fr 2008-06-26  
  256300
FINNISH NEPHROTIC SYNDROME

1 1 3 edith.said@um.edu.mt 2008-08-27  
  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  
  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 X SYNDROME

10 19 10 saker@genethon.fr 2008-06-26  
  193700
FREEMAN-SHELDON SYNDROME

1 4 1 saker@genethon.fr 2008-06-26  
  229300
FRIEDREICH ATAXIA

4 8 4 luisa.politano@unina2.it 2008-06-30  
  229300
FRIEDREICH ATAXIA (UNDEFINED)
G11.1
Early-onset cerebellar ataxia
4 5 5 karcagi.veronika@oki.antsz.hu 2008-07-07  
  229300
FRIEDREICH ATAXIA 1

41 147 49 saker@genethon.fr 2008-06-26  
  229300
FRIEDREICH ATAXIA 1, FRDA
G 11.1
Cerebellar ataxia, Friedreich
17 17 17 mposada@isciii.es 2008-05-30  
  229300
FRIEDREICH ATAXIA; FXA

7 7 marina.fanin@unipd.it 2008-07-04  
  229300
FRIEDRICH ATAXIA
G11.1
Early-onset cerebellar ataxia
3 3 3 mmora@istituto-besta.it 2008-01-09  
  193700
FRREMAN SHELDOM SYNDROME

1 3 1 luisa.politano@unina2.it 2008-06-30  
  253700
GAMMA-SARCOGLYCANOPATHY; LGMD2C
G71.0
30 30 marina.fanin@unipd.it 2008-07-04  
  230500
GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I

8 15 2 edith.said@um.edu.mt 2008-08-27  
  231000
GAUCHER DISEASE, TYPE III
E 75.2
Gaucher, disease
3 3 3 mposada@isciii.es 2008-05-30  
  604233
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES

2 2 1 saker@genethon.fr 2008-06-26  
  231070
GERODERMA OSTEODYSPLASTICA

1 5 1 saker@genethon.fr 2008-06-26  
  256850
GIANT AXONAL NEUROPATHY 1

11 30 19 saker@genethon.fr 2008-06-26  
  137580
GILLES DE LA TOURETTE SYNDROME; GTS
F 95.2
Tourette Syndrome
1 1 1 mposada@isciii.es 2008-05-30  
  231670
GLUTARIC ACIDAEMIA I

1 1 3 edith.said@um.edu.mt 2008-08-27  
  232300
GLYCOGEN STORAGE DISEASE II
E74.0
Glycogen storage disease (Type II)
3 9 3 luisa.politano@unina2.it 2008-06-30  
  232300
GLYCOGEN STORAGE DISEASE II

2 3 3 saker@genethon.fr 2008-06-26  
  300257
GLYCOGEN STORAGE DISEASE IIB

1 1 1 saker@genethon.fr 2008-06-26  
  232400
GLYCOGEN STORAGE DISEASE III

1 1 1 saker@genethon.fr 2008-06-26  
  232600
GLYCOGEN STORAGE DISEASE V

103 122 104 saker@genethon.fr 2008-06-26  
  232300
GLYCOGENOSIS TYPE II

57 57 marina.fanin@unipd.it 2008-07-04  
  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  
  300257
GLYCOGENOSIS TYPE IIB, DANON
G74.0
Glycogen storage disease
1 2 2 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  
  232500
GLYCOGENOSIS TYPE IV
G74.0
Glycogen storage disease
3 3 3 mmora@istituto-besta.it 2008-01-09  
  232600
GLYCOGENOSIS TYPE V, MC ARDLE
G74.0
Glycogen storage disease
21 21 21 mmora@istituto-besta.it 2008-01-09  
  232500
GLYCOGENOSIS TYPE X

3 maurizio.moggio@unimi.it 2008-06-23  
  305600
GOLTZ SYNDROME

2 7 3 saker@genethon.fr 2008-06-26  
  175700
GREIG SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
  141900
HEMOGLOBIN--BETA LOCUS; HBB

22 70 28 edith.said@um.edu.mt 2008-08-27  
  601097
HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSY; HNPP

1 2 2 edith.said@um.edu.mt 2008-08-27  
 
HEREDITARY SPASTIC PARAPLEGIA
G 11.4
Hereditary spastic paraplegia
10 49 38 mposada@isciii.es 2008-05-30  
 
HIDROSADENITIS CHRONIC
L 73.2
Hidrosadenitis chronic
1 1 1 mposada@isciii.es 2008-05-30  
  162500
HNPP

1 1 marina.fanin@unipd.it 2008-07-04  
  236200
HOMOCYSTINURIA

7 19 10 saker@genethon.fr 2008-06-26  
  309900
HUNTER SYNDROME

2 5 3 saker@genethon.fr 2008-06-26  
  143100
HUNTINGTON DISEASE

14 16 14 saker@genethon.fr 2008-06-26  
  143100
HUNTINGTON DISEASE (UNDEFINED)
G10
Huntingon?s disease
5 7 5 karcagi.veronika@oki.antsz.hu 2008-07-07  
  143100
HUNTINGTON DISEASE; HD

13 14 14 edith.said@um.edu.mt 2008-08-27  
  143100
HUNTINGTON DISEASE; HD
G 10
Huntington?s Disease
2 2 2 mposada@isciii.es 2008-05-30  
  607014
HURLER SYNDROME

1 2 1 saker@genethon.fr 2008-06-26  
  176670
HUTCHINSON-GILFORD PROGERIA

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  
  170500
HYPERKALEMIC PERIODIC PARALYSIS

2 2 2 saker@genethon.fr 2008-06-26  
  192600
HYPERTROPHIC CARDIOMYOPATHY

20 29 20 luisa.politano@unina2.it 2008-06-30  
  145900
HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS

145 430 197 saker@genethon.fr 2008-06-26  
  154850
HYPERTROPHY OF MASTICATORY MUSCLES

1 1 1 saker@genethon.fr 2008-06-26  
  240400
HYPOASCORBEMIA

1 1 1 saker@genethon.fr 2008-06-26  
  202400
HYPOFIBRINOGENEMIA, CONGENITAL, INCLUDED
D 68.8
Hypofibrinogenemia
1 1 1 mposada@isciii.es 2008-05-30  
  170400
HYPOKALEMIC PERIODIC PARALYSIS

9 15 12 saker@genethon.fr 2008-06-26  
  170400
HYPOKALIEMIC PERIODIC PARALYSIS
G72.3
Periodic paralysis
11 12 12 mmora@istituto-besta.it 2008-01-09  
  307800
HYPOPHOSPHATEMIA X-LINKED

10 21 11 saker@genethon.fr 2008-06-26  
 
IBM

8 maurizio.moggio@unimi.it 2008-06-23  
  146800
ICHTHYOSIFORM ERYTHRODERMA, BULLOUS
Q80.3
Congenital bullous ichthyosiform erythroderma
3 4 4 mposada@isciii.es 2008-05-30  
  242100
ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL, NONBULLOUS
Q 80
Congenital ichthyosis
2 4 4 mposada@isciii.es 2008-05-30  
  146800
ICHTHYOSIS BULLOUS TYPE

1 3 1 saker@genethon.fr 2008-06-26  
  242500
ICHTHYOSIS CONGENITA HARLEQUIN FETUS TYPE

3 12 3 saker@genethon.fr 2008-06-26  
  308205
ICHTHYOSIS FOLLICULARIS ATRICHIA AND PHOTOPHOBIA SYNDROME

1 4 2 saker@genethon.fr 2008-06-26  
  146590
ICHTHYOSIS HYSTRIX, CURTH-MACKLIN TYPE

3 22 9 saker@genethon.fr 2008-06-26  
  146750
ICHTHYOSIS LAMELLAR , AUTOSOMAL DOMINANT FORM

3 15 11 saker@genethon.fr 2008-06-26  
  242300
ICHTHYOSIS LAMELLAR 1, COLLODION BABY

218 1113 313 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  
  308100
ICHTHYOSIS X-LINKED

12 50 20 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  
  269920
INFANTILE SIALIC ACID STORAGE DISORDER

1 3 1 saker@genethon.fr 2008-06-26  
  308350
INFANTILE SPASM SYNDROME- WEST SYNDROME

3 12 5 saker@genethon.fr 2008-06-26  
  308370
INFERTILE MALE SYNDROME

2 2 2 saker@genethon.fr 2008-06-26  
  243180
INTESTINAL PSEUDOOBSTRUCTION DISEASE

18 56 19 saker@genethon.fr 2008-06-26  
  605479
INTRAEPATIC CHOLESTASIS 2

1 1 1 luisa.politano@unina2.it 2008-07-07  
  600546
INTRAUTERINE GROWTH RETARDATION- SECKEL SYNDROME

3 14 4 saker@genethon.fr 2008-06-26  
  204500
JANSKY-BIELSCHOWSKY DISEASE

5 22 5 saker@genethon.fr 2008-06-26  
  213300
JOUBERT SYNDROME

3 10 4 saker@genethon.fr 2008-06-26  
  606904
JUVENILE MYOCLONIC EPILEPSY

92 513 200 saker@genethon.fr 2008-06-26  
  244200
KALLMANN SYNDROME 3

1 4 2 saker@genethon.fr 2008-06-26  
  148000
KAPOSI SARCOMA

1 1 1 luisa.politano@unina2.it 2008-06-30  
  148000
KAPOSI SARCOMA

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

15 15 marina.fanin@unipd.it 2008-07-04  
  148210
KERATITIS ICHTHYOSIS DEAFNESS SYNDROME

2 9 2 saker@genethon.fr 2008-06-26  
  308800
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS

1 7 2 saker@genethon.fr 2008-06-26  
  601952
KERATOSIS LINEARIS WITH ICHTHYOSIS CONGENITA AND SCLEROSING KERATODERMA

1 9 1 saker@genethon.fr 2008-06-26  
  148600
KERATOSIS PALMOPLANTARIS PAPULOSA

2 4 3 saker@genethon.fr 2008-06-26  
  245150
KEUTEL SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
  173650
KINDLER SYNDROME

7 27 10 saker@genethon.fr 2008-06-26  
  267750
KNOBLOCH SYNDROME
H54.0
Blidness, both eyes
1 9 2 karcagi.veronika@oki.antsz.hu 2008-07-07  
  253400
KUGELBERG-WELANDER;SMA3

18 18 marina.fanin@unipd.it 2008-07-04  
  604777
LAMELLAR ICHTHYOSIS TYPE 3

1 2 1 saker@genethon.fr 2008-06-26  
  159001
LAMINOPATHY; LMNA
G71.0
16 16 marina.fanin@unipd.it 2008-07-04  
  150230
LANGER-GIEDION SYNDROME

1 4 1 saker@genethon.fr 2008-06-26  
  604856
LANGERHANS CELL HISTIOCYTOSIS

98 102 98 saker@genethon.fr 2008-06-26  
  262500
LARON SYNDROME

30 93 41 saker@genethon.fr 2008-06-26  
  245800
LAURENCE-MOON SYNDROME

5 13 5 saker@genethon.fr 2008-06-26  
  535000
LEBER

37 maurizio.moggio@unimi.it 2008-06-23  
  204000
LEBER CONGENITAL AMAUROSIS
H35.5
Leber's Congenital Amaurosis
1 1 1 mposada@isciii.es 2008-05-30  
  535000
LEBER OPTIC ATROPHY

14 54 21 saker@genethon.fr 2008-06-26  
  256000
LEIGH SYNDROME

3 6 3 saker@genethon.fr 2008-06-26  
  150800
LEIOMYOMA OF SKIN

1 8 5 saker@genethon.fr 2008-06-26  
  151001
LENTIGINOSIS

1 1 1 saker@genethon.fr 2008-06-26  
  300322
LESCH NYAN SYNDROME

1 6 3 luisa.politano@unina2.it 2008-06-30  
  308000
LESCH-NYHAN SYNDROME (UNDEFINED)
E79.1
Lesch-Nyhan syndrome
2 1 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  259775
LETHAL OSTEOSCLEROTIC BONE DYSPLASIA, RAINE SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
  253600
LGMD (UNDEFINED)
G71.0
Muscular dystrophy
33 60 34 karcagi.veronika@oki.antsz.hu 2008-07-07  
  159001
LGMD1B, LMNA
G71.0
Muscular dystrophy
6 6 6 mmora@istituto-besta.it 2008-01-09  
  607801
LGMD1C, CAVEOLINOPATHY

60 maurizio.moggio@unimi.it 2008-06-23  
  607801
LGMD1C, CAVEOLINOPATHY
G71.0
Muscular dystrophy
4 10 10 mmora@istituto-besta.it 2008-01-09  
  253600
LGMD2A, CALPAINOPATHY

46 maurizio.moggio@unimi.it 2008-06-23  
  253600
LGMD2A, CALPAINOPATHY
G71.0
Muscular dystrophy
18 20 20 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  
  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  
  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  
  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  
  601287
LGMD2F, DELTA-SARCOGLYCANOPATHY

maurizio.moggio@unimi.it 2008-06-23  
  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  
  535000
LHON-LEBER OPTIC ATROPHY (DEFINED)
H47.2
Optic atrophy
22 55 36 karcagi.veronika@oki.antsz.hu 2008-07-07  
  535000
LHON-LEBER OPTIC ATROPHY (UNDEFINED)
H47.2
Optic atrophy
120 161 132 karcagi.veronika@oki.antsz.hu 2008-07-07  
  607155
LIMB-GIRDLE DYSTROPHY 2I;LGMD2I
G71.0
51 51 marina.fanin@unipd.it 2008-07-04  
 
LIPID STORAGE MYOPATHY
E75.6
Lipid storage disorder, unspecified
40 40 40 mmora@istituto-besta.it 2008-01-09  
  255100
LIPID STORAGE MYOPATHY

9 9 9 luisa.politano@unina2.it 2008-06-30  
 
LIPID STORAGE MYOPATHY

4 maurizio.moggio@unimi.it 2008-06-23  
  608056
LIPOATROPHY WITH DIABETES HEPATIC STEATOSIS

1 2 2 saker@genethon.fr 2008-06-26  
  151900
LIPOMATOSIS MULTIPLE

1 1 1 saker@genethon.fr 2008-06-26  
  151800
LIPOMATOSIS, FAMILIAL BENIGN CERVICAL
E 88.2
Lipomatosis
1 1 1 mposada@isciii.es 2008-05-30  
  607432
LISSENCEPHALY

9 21 4 saker@genethon.fr 2008-06-26  
  152460
LOBULAR GLOMERULOPATHY FAMILIAL

1 28 9 saker@genethon.fr 2008-06-26  
  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  
  247200
LYSSENCEPHALIA (MDLS) (UNDEFINED)
G30-G32
Other degenerative disease of the nervous system
1 2 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  109150
MACHADO JOSEPH DISEASE, MJD

1 1 1 mposada@isciii.es 2008-05-30  
  153700
MACULAR DYSTROPHY, VITELLIFORM

1 4 1 saker@genethon.fr 2008-06-26  
 
MAD DEFICIENCY

6 maurizio.moggio@unimi.it 2008-06-23  
  248300
MAL DE MELEDA

48 304 93 saker@genethon.fr 2008-06-26  
  145600
MALIGNANT HYPERTHERMIA
T88.3
Malignant hyperthermia
3 3 3 luisa.politano@unina2.it 2008-06-30  
 
MALIGNANT HYPERTHERMIA

192 maurizio.moggio@unimi.it 2008-06-23  
  117000
MALIGNANT HYPERTHERMIA, CCD;MH

1 1 marina.fanin@unipd.it 2008-07-04  
  145600
MALIGNANT HYPERTHERMIA;MH

2 2 marina.fanin@unipd.it 2008-07-04  
  125480
MANIC-DEPRESSIVE PSYCHOSIS

49 199 81 saker@genethon.fr 2008-06-26  
  248700
MARDEN-WALKER SYNDROME

1 2 2 saker@genethon.fr 2008-06-26  
  154700
MARFAN SYNDROME

9 13 12 saker@genethon.fr 2008-06-26  
 
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  
 
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  
  248800
MARINESCO-SJOGREN SYNDROME

3 14 8 saker@genethon.fr 2008-06-26  
  232600
MC ARDLE DISEASE

16 16 marina.fanin@unipd.it 2008-07-04  
  604004
MEGALENCEPHALIC LEUKOENCEPHALOPATHY WITH SUBCORTICAL CYSTS

27 125 29 saker@genethon.fr 2008-06-26  
  540000
MELAS

38 maurizio.moggio@unimi.it 2008-06-23  
  540000
MELAS
G71.3
45 45 marina.fanin@unipd.it 2008-07-04  
 
MELAS/MERRF
G71.3
Mitochondrial myopathy, not elsewhere classified
37 37 37 mmora@istituto-besta.it 2008-01-09  
  309400
MENKES DISEASE

2 4 2 saker@genethon.fr 2008-06-26  
  607855
MEROSINOPATHY, LAMA2
G71.2
Congenital myopathies
21 22 22 mmora@istituto-besta.it 2008-01-09  
  156225
MEROSINOPATHY;LAMA2
G71.0
23 23 marina.fanin@unipd.it 2008-07-04  
  545000
MERRF
G71.3
2 2 marina.fanin@unipd.it 2008-07-04  
  545000
MERRF

38 maurizio.moggio@unimi.it 2008-06-23  
  250100
METACHROMATIC LEUKODYSTROPHY

2 8 3 saker@genethon.fr 2008-06-26  
  251200
MICROCEPHALY

3 3 3 saker@genethon.fr 2008-06-26  
 
MILD NON SPECIFIC MYOPATHIC SIGNS

777 maurizio.moggio@unimi.it 2008-06-23  
  255320
MINICORE DISEASE

1 1 1 luisa.politano@unina2.it 2008-06-30  
 
MINICORE MYOPATHY
G71.2
Congenital myopathies
7 7 7 mmora@istituto-besta.it 2008-01-09  
  255320
MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA (UNDEFINED)
G71.2
Congenital myopathies
2 6 4 karcagi.veronika@oki.antsz.hu 2008-07-07  
  251900
MITOCHONDRIAL MYOPATHY

25 42 31 saker@genethon.fr 2008-06-26  
  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  
  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  
 
MITOCHONDRIAL-LIPID-GLYCOGEN STORAGE
G71.3
Mitochondrial myopathy, not elsewhere classified
1 1 1 mmora@istituto-besta.it 2008-01-09  
  157900
MOEBIUS SYNDROME

2 2 2 saker@genethon.fr 2008-06-26  
 
MTDNA DEPLETION

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

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

130 maurizio.moggio@unimi.it 2008-06-23  
  191900
MUCKLE-WELLS SYNDROME

5 26 12 saker@genethon.fr 2008-06-26  
  255320
MULTIMINICORE DISEASE

96 311 106 saker@genethon.fr 2008-06-26  
  126200
MULTIPLE SCLEROSIS

38 236 88 saker@genethon.fr 2008-06-26  
  126200
MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO; MS

65 65 65 edith.said@um.edu.mt 2008-08-27  
  186600
MULTIPLE SYRINGOMAS

2 7 3 saker@genethon.fr 2008-06-26  
  253280
MUSCLE-EYE-BRAIN DISEASE

4 9 3 saker@genethon.fr 2008-06-26  
  300376
MUSCULAR DYSTROPHY BECKER TYPE

25 37 27 saker@genethon.fr 2008-06-26  
  310200
MUSCULAR DYSTROPHY DUCHENNE TYPE

56 86 58 saker@genethon.fr 2008-06-26  
  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  
  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  
  310200
MUSCULAR DYSTROPHY, DUCHENNE TYPE, DMD
G 71.0
Muscular Dystrophy
2 2 2 mposada@isciii.es 2008-05-30  
  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  
  607801
MUSCULAR DYSTROPHY, LIMB-GIRDLE TYPE 1C

5 5 5 saker@genethon.fr 2008-06-26  
  253600
MUSCULAR DYSTROPHY, LIMB-GIRDLE TYPE 2A

63 370 119 saker@genethon.fr 2008-06-26  
  253700
MUSCULAR DYSTROPHY, LIMB-GIRDLE TYPE 2C

47 164 86 saker@genethon.fr 2008-06-26  
  159001
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B; LGMD1B
G71.0
Muscular dystrophy (LGMD 1B)
11 13 13 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  
  253600
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A
G71.0
Muscular dystrophy (LGMD 2A)
93 102 100 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  
  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  
  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  
  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 2F; LGMD2F
G71.0
Muscular dystrophy (LGMD 2F with mutation in delta-SG)
1 12 2 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  
  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  
 
MYASTENIC SYNDROME
G70.2
Congenital and developmental myasthenia
2 4 2 mmora@istituto-besta.it 2008-01-09  
  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  
  545000
MYOCLONIC EPILEPSY (UNDEFINED)
G40.3
Generalized idiopathic epilepsy and epileptic syndromes
2 2 2 karcagi.veronika@oki.antsz.hu 2008-07-07  
  254780
MYOCLONIC EPILEPSY OF LAFORA

15 58 16 saker@genethon.fr 2008-06-26  
 
MYOFIBRILLAR MYOPATHIES

maurizio.moggio@unimi.it 2008-06-23  
  158810
MYOPATHY BENIGN CONGENITAL WITH CONTRACTURES

28 70 38 saker@genethon.fr 2008-06-26  
  601419
MYOPATHY DESMIN RELATED

32 136 52 saker@genethon.fr 2008-06-26  
  160300
MYOPATHY DISTAL

161 322 185 saker@genethon.fr 2008-06-26  
  160500
MYOPATHY DISTAL 1

1 4 3 saker@genethon.fr 2008-06-26  
  102770
MYOPATHY DUE TO MYOADENYLATE DEAMINASE DEFICIENCY

1 1 1 saker@genethon.fr 2008-06-26  
  310440
MYOPATHY WITH EXCESSIVE AUTOPHAGY

2 3 3 saker@genethon.fr 2008-06-26  
  160150
MYOPATHY, CENTRONUCLEAR (UNDEFINED)
G71.2
Congenital myopathies
1 5 1 karcagi.veronika@oki.antsz.hu 2008-07-07  
  160565
MYOPATHY, TUBULAR AGGEGATES
G71.3
Mitochondrial Myopathy (with tubular aggregates)
1 1 1 luisa.politano@unina2.it 2008-06-30  
  160800
MYOTONIA CONGENITA- THOMSEN DISEASE

67 103 76 saker@genethon.fr 2008-06-26  
  255700
MYOTONIA CONGENITA, AUTOSOMAL-RECESSIVE
G71.1
Recessive myotonia congenita (Becker)
1 1 luisa.politano@unina2.it 2008-06-30  
  602668
MYOTONIC DYSTROPHY TYPE 2, PROMM, DM2
G71.1
Myotonic disorders
5 5 5 mmora@istituto-besta.it 2008-01-09  
  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; DM2
G71.1
11 11 marina.fanin@unipd.it 2008-07-04  
  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  
  310400
MYOTUBULAR MYOPATHY

27 105 25 saker@genethon.fr 2008-06-26  
  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, MTMX
G71.2
Congenital myopathies
1 1 1 mmora@istituto-besta.it 2008-01-09  
  551500
NARP

3 maurizio.moggio@unimi.it 2008-06-23  
 
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  
  161800
NEMALINE MYOPATHY 3; NEM3 (DEFINED)
G72.9
other myopathies
2 2 2 karcagi.veronika@oki.antsz.hu 2008-07-07  
  161800
NEMALINE MYOPATHY 3; NEM3 (UNDEFINED)
G72.9
other myopathies
2 6 2 karcagi.veronika@oki.antsz.hu 2008-07-07  
  256030
NEMALINE MYOPATHY; NEM2

3 3 marina.fanin@unipd.it 2008-07-04  
  194070
NEPHROBLASTOMA

15 18 16 saker@genethon.fr 2008-06-26  
  256500
NETHERTON SYNDROME

9 36 10 saker@genethon.fr 2008-06-26  
  256600
NEUROAXONAL DYSTROPHY INFANTILE

3 9 6 saker@genethon.fr 2008-06-26  
  162200
NEUROFIBROMATOSIS

14 20 13 saker@genethon.fr 2008-06-26  
  162200
NEUROFIBROMATOSIS 1

1 1 1 luisa.politano@unina2.it 2008-07-07  
  162200
NEUROFIBROMATOSIS, TYPE I; NF1

2 4 1 edith.said@um.edu.mt 2008-08-27  
  607379
NEUROFIBROMIN 2

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

1 3 2 saker@genethon.fr 2008-06-26  
  223900
NEUROPATHY HEREDITARY SENSORY AND AUTONOMIC TYPE III

1 1 1 saker@genethon.fr 2008-06-26  
  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  
  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  
  605275
NOONAN SYNDROME 2

2 12 4 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  
  602025
OBESITY

227 429 13 saker@genethon.fr 2008-06-26  
  164210
OCULOAURICULOVERTEBRAL DYSPLASIA-GOLDENHAR SYNDROME

1 1 1 saker@genethon.fr 2008-06-26  
  164300
OCULO-PHARYNGEAL

3 maurizio.moggio@unimi.it 2008-06-23  
  164300
OCULO-PHARYNGEAL DYSTROPHY
G71.0
Muscular dystrophy
22 22 22 mmora@istituto-besta.it 2008-01-09  
  164300
OCULOPHARYNGEAL MD, OPMD

1 1 1 luisa.politano@unina2.it 2008-07-07  
  164300
OCULOPHARYNGEAL MUSCULAR DYSTROPHY

143 301