|
spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy
|
33043 |
|
|
spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy; SPAX8
|
http://purl.obolibrary.org/obo/MONDO_0033043 |
|
|
Meier-Gorlin syndrome 8; MGORS8
|
http://purl.obolibrary.org/obo/MONDO_0033046 |
|
|
von Willebrand disease type 2
|
13304 |
|
|
von willebrand's disease 2
|
13304 |
|
|
orofaciodigital syndrome XVI
|
33045 |
|
|
orofaciodigital syndrome XVI; OFD16
|
http://purl.obolibrary.org/obo/MONDO_0033045 |
|
|
nonsyndromic deafness, Y-linked
|
33304 |
|
|
von Willebrand's disease type 2
|
13304 |
|
|
von Willebrand disease type II
|
13304 |
|
