Search results for "[genes] MYH9"

14 hits were found for '[genes] MYH9'

# Family MCID Name MIFTS Score
1
FCH003 Fechtner Syndrome 38 34.522
2
EPS006 Epstein Syndrome 28 34.522
3
SBS006 Sebastian Syndrome 25 34.522
4
MYH001 May-Hegglin Anomaly 39 28.187
5
MYH002 Myh9-Related Disorders 18 23.015
6
P ALP004 Alport Syndrome 60 19.931
7
MCR139 Macrothrombocytopenia and Progressive Sensorineural Deafness 16 18.195
8
P ATS208 Autosomal Dominant Macrothrombocytopenia 27 16.274
9
c DFN200 Deafness, Autosomal Dominant 17 11 14.094
10
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 28 8.137
11
c MYH004 Myh9 Related Thrombocytopenia 22 8.137
12
P DFN023 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 17 13 8.137
13
MCR041 Macrothrombocytopenia Progressive Deafness 5 8.137
14
DFN052 Dfna17 Nonsyndromic Hearing Loss and Deafness 4 8.137