|
spermatogenic failure 7; SPGF7
|
http://purl.obolibrary.org/obo/MONDO_0013070 |
|
|
cardiomyopathy, dilated, 1c
|
C563307 |
|
|
autosomal dominant Emery-Dreifuss muscular dystrophy caused by mutation in SYNE1
|
13071 |
|
|
autosomal dominant Emery-Dreifuss muscular dystrophy caused by mutation in SYNE2
|
13072 |
|
|
immunodeficiencies, x-linked Hyper-IgM
|
D053307 |
|
|
autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B
|
7307 |
|
|
Dowling-Degos disease 4; DDD4
|
http://purl.obolibrary.org/obo/MONDO_0014307 |
|
|
immunodeficiency, x-linked Hyper-IgM
|
D053307 |
|
|
type 1 Hyper-IgM immunodeficiency syndrome
|
D053307 |
|
|
immunodeficiency with Hyper-IgM, type 1
|
D053307 |
|
|
Zazam Sheriff Phillips syndrome
|
43071 |
|
|
x-linked hyper IgM syndrome
|
D053307 |
|
