|
myocardial infarction (disease), acute
|
4781 |
|
|
ebv-associated, autosomal, 1 lymphoproliferative syndrome
|
C567815 |
|
|
maternal monosomy 14q32.2
|
16781 |
|
|
spinocerebellar ataxia 17
|
11781 |
|
|
spinocerebellar ataxia 17; SCA17
|
http://purl.obolibrary.org/obo/MONDO_0011781 |
|
|
pseudohypoaldosteronism type 2 caused by mutation in KLHL3
|
13781 |
|
|
pseudohypoaldosteronism type 2D
|
13781 |
|
|
pseudohypoaldosteronism, type 2D
|
13781 |
|
|
Oral-facial-digital syndrome 3
|
C557817 |
|
|
Huntington disease-like 4
|
11781 |
|
|
Oral-facial-digital syndrome 5
|
C557819 |
|
