|
eyelid hypertrichosis (disease)
|
1334 |
|
|
hereditary hyperlipidemia (disease)
|
1336 |
|
|
vesicoureteral reflux (disease) caused by mutation in SOX17
|
13356 |
|
|
cone-ROD dystrophy 15; CORD15
|
http://purl.obolibrary.org/obo/MONDO_0013348 |
|
|
Glanzmann thrombasthenia 1
|
31332 |
|
|
brachyolmia type 2; BCYM2
|
http://purl.obolibrary.org/obo/MONDO_0013360 |
|
|
familial persistent 1 stuttering
|
D013342 |
|
|
spinocerebellar ataxia 10
|
11330 |
|
|
orofacial cleft 10; OFC10
|
http://purl.obolibrary.org/obo/MONDO_0013378 |
|
|
spinocerebellar ataxia 10; SCA10
|
http://purl.obolibrary.org/obo/MONDO_0011330 |
|
