Search results for "[genes] GJA1"

36 hits were found for '[genes] GJA1'

# Family MCID Name MIFTS Score
1
P OCL013 Oculodentodigital Dysplasia 59 28.244
2
c SYN060 Syndactyly, Type Iii 29 20.626
3
P HYP055 Hypoplastic Left Heart Syndrome 62 19.294
4
P CRN012 Craniometaphyseal Dysplasia 51 19.294
5
P SYN001 Syndactyly 48 19.294
6
ERY021 Erythrokeratodermia Variabilis Et Progressiva 46 19.294
7
c CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 28 19.294
8
c ATR064 Atrioventricular Septal Defect 3 24 19.294
9
c HYP543 Hypoplastic Left Heart Syndrome 1 27 17.863
10
P HLL001 Hallermann-Streiff Syndrome 55 16.307
11
c OCL047 Oculodentodigital Dysplasia, Autosomal Recessive 27 16.307
12
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 54 14.585
13
P HYP087 Hypotrichosis 44 14.585
14
TTR001 Tetralogy of Fallot 70 12.631
15
P CRD011 Cardiomyopathy 68 12.631
16
P HYP061 Hypertrophic Cardiomyopathy 63 12.631
17
P ATR001 Atrioventricular Septal Defect 55 12.631
18
P PLM140 Palmoplantar Keratoderma with Congenital Alopecia 26 12.631
19
DBT062 Diabetic Foot Ulcers 64 10.313
20
GLS001 Gliosarcoma 59 10.313
21
ECT078 Ectodermal Dysplasia 2, Clouston Type 49 10.313
22
c SPN312 Spinocerebellar Ataxia 14 48 10.313
23
BSL006 Basaloid Squamous Cell Carcinoma 47 10.313
24
SKN005 Skin Atrophy 47 10.313
25
HRT008 Heart Conduction Disease 44 10.313
26
TRC021 Tricuspid Valve Stenosis 43 10.313
27
c CHR054 Chronic Closed-Angle Glaucoma 42 10.313
28
DNT007 Dentin Sensitivity 41 10.313
29
KRT011 Keratitis-Ichthyosis-Deafness Syndrome 39 10.313
30
BRT001 Bart-Pumphrey Syndrome 37 10.313
31
LKN007 Leukonychia Totalis 30 10.313
32
c PLZ002 Pelizaeus-Merzbacher-Like Disease 29 10.313
33
CRS011 Criss-Cross Heart 23 10.313
34
HYP659 Hypomyelinating Leukoencephalopathy 21 10.313
35
ATS252 Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb 24 7.293
36
c ATS068 Autosomal Dominant Palmoplantar Keratoderma and Congenital Alopecia 13 7.293