Search results for "[genes] GJA1"

45 hits were found for '[genes] GJA1'

# Family MCID Name MIFTS Score
1
P OCL013 Oculodentodigital Dysplasia 59 27.252
2
c SYN060 Syndactyly, Type Iii 26 19.902
3
P HYP055 Hypoplastic Left Heart Syndrome 60 18.617
4
ERY021 Erythrokeratodermia Variabilis Et Progressiva 48 18.617
5
P CRN012 Craniometaphyseal Dysplasia 47 18.617
6
c CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 23 18.617
7
c ATR064 Atrioventricular Septal Defect 3 17 18.617
8
P HRT032 Heart Disease 76 17.236
9
c HYP543 Hypoplastic Left Heart Syndrome 1 21 17.236
10
P HLL001 Hallermann-Streiff Syndrome 53 15.734
11
c OCL047 Oculodentodigital Dysplasia, Autosomal Recessive 21 15.734
12
ALP008 Alopecia 55 14.073
13
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 55 14.073
14
P HYP087 Hypotrichosis 45 14.073
15
P PLM140 Palmoplantar Keratoderma with Congenital Alopecia 21 14.073
16
P MYC007 Myocardial Infarction 79 12.187
17
c DLT002 Dilated Cardiomyopathy 75 12.187
18
TTR001 Tetralogy of Fallot 71 12.187
19
SKN016 Skin Disease 68 12.187
20
P CRD011 Cardiomyopathy 67 12.187
21
P ATR001 Atrioventricular Septal Defect 52 12.187
22
CRN245 Craniosynostosis, Philadelphia Type 50 12.187
23
KRT009 Keratosis 50 12.187
24
GLS001 Gliosarcoma 55 9.951
25
c SPN312 Spinocerebellar Ataxia 14 46 9.951
26
LMB050 Limbal Stem Cell Deficiency 45 9.951
27
ECT078 Ectodermal Dysplasia 2, Clouston Type 45 9.951
28
SKN005 Skin Atrophy 43 9.951
29
TST043 Testicular Seminoma 40 9.951
30
BRT001 Bart-Pumphrey Syndrome 40 9.951
31
TRC021 Tricuspid Valve Stenosis 39 9.951
32
DNT007 Dentin Sensitivity 38 9.951
33
c CHR054 Chronic Closed-Angle Glaucoma 38 9.951
34
KRT011 Keratitis-Ichthyosis-Deafness Syndrome 37 9.951
35
SNT005 Sinoatrial Node Disease 35 9.951
36
ANH001 Ainhum 29 9.951
37
c PLZ002 Pelizaeus-Merzbacher-Like Disease 26 9.951
38
PSD026 Pseudoainhum 23 9.951
39
CRS011 Criss-Cross Heart 19 9.951
40
LKN007 Leukonychia Totalis 18 9.951
41
HYP659 Hypomyelinating Leukoencephalopathy 16 9.951
42
ANM031 Anomalous Left Coronary Artery from the Pulmonary Artery 16 9.951
43
P RTH001 Rothmund-Thomson Syndrome 57 7.036
44
HRT008 Heart Conduction Disease 43 7.036
45
ATS252 Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb 24 7.036