Search results for "[genes] GJA1"

36 hits were found for '[genes] GJA1'

# Family MCID Name MIFTS Score
1
P OCL013 Oculodentodigital Dysplasia 56 28.244
2
c SYN060 Syndactyly, Type Iii 29 20.626
3
P HYP055 Hypoplastic Left Heart Syndrome 59 19.294
4
P CRN012 Craniometaphyseal Dysplasia 53 19.294
5
P SYN001 Syndactyly 48 19.294
6
ERY021 Erythrokeratodermia Variabilis Et Progressiva 47 19.294
7
c CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 27 19.294
8
c ATR064 Atrioventricular Septal Defect 3 20 19.294
9
c HYP543 Hypoplastic Left Heart Syndrome 1 21 17.863
10
P HLL001 Hallermann-Streiff Syndrome 54 16.307
11
c OCL047 Oculodentodigital Dysplasia, Autosomal Recessive 27 16.307
12
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 51 14.585
13
P HYP087 Hypotrichosis 36 14.585
14
TTR001 Tetralogy of Fallot 66 12.631
15
P CRD011 Cardiomyopathy 59 12.631
16
P HYP061 Hypertrophic Cardiomyopathy 55 12.631
17
P ATR001 Atrioventricular Septal Defect 50 12.631
18
P PLM140 Palmoplantar Keratoderma with Congenital Alopecia 22 12.631
19
ECT078 Ectodermal Dysplasia 2, Clouston Type 50 10.313
20
DBT062 Diabetic Foot Ulcers 50 10.313
21
GLS001 Gliosarcoma 46 10.313
22
c SPN312 Spinocerebellar Ataxia 14 45 10.313
23
BSL006 Basaloid Squamous Cell Carcinoma 40 10.313
24
BRT001 Bart-Pumphrey Syndrome 38 10.313
25
KRT011 Keratitis-Ichthyosis-Deafness Syndrome 38 10.313
26
TRC021 Tricuspid Valve Stenosis 37 10.313
27
SKN005 Skin Atrophy 36 10.313
28
c CHR054 Chronic Closed-Angle Glaucoma 34 10.313
29
HRT008 Heart Conduction Disease 34 10.313
30
DNT007 Dentin Sensitivity 32 10.313
31
LKN007 Leukonychia Totalis 30 10.313
32
c PLZ002 Pelizaeus-Merzbacher-Like Disease 28 10.313
33
CRS011 Criss-Cross Heart 25 10.313
34
HYP659 Hypomyelinating Leukoencephalopathy 18 10.313
35
ATS252 Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb 22 7.293
36
c ATS068 Autosomal Dominant Palmoplantar Keratoderma and Congenital Alopecia 12 7.293