Search results for "GJA1"

38 hits were found for 'GJA1'

# Family MCID Name MIFTS Score
1
P OCL013 Oculodentodigital Dysplasia 57 10.329
2
P HYP055 Hypoplastic Left Heart Syndrome 68 5.927
3
c SYN060 Syndactyly, Type Iii 30 4.963
4
P SYN001 Syndactyly 50 4.580
5
P CRN012 Craniometaphyseal Dysplasia 57 4.523
6
c HYP543 Hypoplastic Left Heart Syndrome 1 22 4.244
7
c ATR064 Atrioventricular Septal Defect 3 17 4.244
8
c OCL047 Oculodentodigital Dysplasia, Autosomal Recessive 21 3.818
9
GLS001 Gliosarcoma 60 3.693
10
c CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 30 3.693
11
P DLT002 Dilated Cardiomyopathy 86 2.612
12
HLY001 Hailey-Hailey Disease 68 2.612
13
P GLB002 Glioblastoma 67 2.612
14
c FML058 Familial Dilated Cardiomyopathy 66 2.612
15
P HLL001 Hallermann-Streiff Syndrome 60 2.612
16
P ATR001 Atrioventricular Septal Defect 56 2.612
17
HTR003 Heterotaxy 56 2.612
18
BRN032 Brain Glioma 48 2.612
19
DBT062 Diabetic Foot Ulcers 46 2.612
20
SKN005 Skin Atrophy 39 2.612
21
c PLZ002 Pelizaeus-Merzbacher-Like Disease 33 2.612
22
DNT013 Dental Enamel Hypoplasia 27 2.612
23
CRS011 Criss-Cross Heart 26 2.612
24
ATS252 Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb 32 1.847
25
KRT012 Keratoderma 45 0.130
26
DCH001 Duchenne Muscular Dystrophy 80 0.075
27
BCK001 Becker Muscular Dystrophy 62 0.075
28
CRV038 Cervical Squamous Cell Carcinoma 52 0.075
29
ERY021 Erythrokeratodermia Variabilis Et Progressiva 48 0.075
30
KRT009 Keratosis 48 0.075
31
PRP016 Paraplegia 46 0.075
32
P HYP087 Hypotrichosis 41 0.075
33
c NNS007 Nonsyndromic Deafness 39 0.075
34
PLM029 Palmoplantar Keratosis 38 0.075
35
SPS057 Spasticity 37 0.075
36
CHL028 Childhood Type Dermatomyositis 36 0.075
37
LKN007 Leukonychia Totalis 30 0.075
38
c EMR003 Emery-Dreifuss Muscular Dystrophy, Dominant Type 11 0.075