Search results for "[genes] GJA1"

38 hits were found for '[genes] GJA1'

# Family MCID Name MIFTS Score
1
P OCL013 Oculodentodigital Dysplasia 57 28.943
2
P HYP055 Hypoplastic Left Heart Syndrome 58 20.466
3
P CRN012 Craniometaphyseal Dysplasia 53 20.466
4
c SYN060 Syndactyly, Type Iii 30 20.466
5
P SYN001 Syndactyly 49 19.144
6
c CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 28 19.144
7
c ATR064 Atrioventricular Septal Defect 3 21 19.144
8
ERY021 Erythrokeratodermia Variabilis Et Progressiva 50 17.724
9
c HYP543 Hypoplastic Left Heart Syndrome 1 23 17.724
10
P HLL001 Hallermann-Streiff Syndrome 53 16.179
11
c OCL047 Oculodentodigital Dysplasia, Autosomal Recessive 27 16.179
12
MLG068 Malignant Glioma 57 14.471
13
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 47 14.471
14
P HYP087 Hypotrichosis 38 14.471
15
P MYC007 Myocardial Infarction 76 12.533
16
c DLT002 Dilated Cardiomyopathy 73 12.533
17
TTR001 Tetralogy of Fallot 68 12.533
18
P HYP061 Hypertrophic Cardiomyopathy 56 12.533
19
P CRD011 Cardiomyopathy 53 12.533
20
P ATR001 Atrioventricular Septal Defect 45 12.533
21
KRT009 Keratosis 43 12.533
22
ECT078 Ectodermal Dysplasia 2, Clouston Type 49 10.233
23
GLS001 Gliosarcoma 45 10.233
24
KRT011 Keratitis-Ichthyosis-Deafness Syndrome 40 10.233
25
DBT062 Diabetic Foot Ulcers 40 10.233
26
TRC021 Tricuspid Valve Stenosis 38 10.233
27
LMB050 Limbal Stem Cell Deficiency 38 10.233
28
BRT001 Bart-Pumphrey Syndrome 36 10.233
29
SKN005 Skin Atrophy 34 10.233
30
c CHR054 Chronic Closed-Angle Glaucoma 31 10.233
31
DNT007 Dentin Sensitivity 27 10.233
32
LKN007 Leukonychia Totalis 27 10.233
33
c PLZ002 Pelizaeus-Merzbacher-Like Disease 26 10.233
34
PSD026 Pseudoainhum 23 10.233
35
P PLM140 Palmoplantar Keratoderma with Congenital Alopecia 22 10.233
36
CRS011 Criss-Cross Heart 22 10.233
37
c ATS068 Autosomal Dominant Palmoplantar Keratoderma and Congenital Alopecia 12 10.233
38
ATS252 Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb 25 7.236