|
mitochondrial complex 3 deficiency, nuclear type 10
|
32909 |
|
|
HUMAN HERPESVIRUS 8, susceptibility to
|
13909 |
|
|
human herpesvirus 8, susceptibility to
|
13909 |
|
|
HUMAN HERPESVIRUS 8, susceptibility to; HHV8S
|
http://purl.obolibrary.org/obo/MONDO_0013909 |
|
|
Schofer Beetz Bohl syndrome
|
9099 |
|
|
MPZ-related intermediate Charcot-Marie-Tooth neuropathy
|
11909 |
|
|
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 10
|
32909 |
|
|
dementia, familial, Neumann type
|
9096 |
|
|
familial dementia, Neumann type
|
9096 |
|
|
Charcot Marie Tooth disease dominant intermediate 3
|
11909 |
|
|
intellectual disability, X-linked, syndromic, HOUGE type
|
30909 |
|
|
mental retardation, X-linked, syndromic, HOUGE type
|
30909 |
|
|
mental retardation, X-linked, syndromic, HOUGE type; MRXSHG
|
http://purl.obolibrary.org/obo/MONDO_0030909 |
|
