|
autosomal dominant nonsyndromic deafness 51
|
13305 |
|
|
autosomal dominant nonsyndromic deafness type 51
|
13305 |
|
|
combined oxidative phosphorylation deficiency 7
|
13306 |
|
|
combined oxidative phosphorylation deficiency 7; COXPD7
|
http://purl.obolibrary.org/obo/MONDO_0013306 |
|
|
combined oxidative phosphorylation deficiency caused by mutation in C12ORF65
|
13306 |
|
|
combined oxidative phosphorylation deficiency caused by mutation in C12orf65
|
13306 |
|
|
combined oxidative phosphorylation deficiency type 7
|
13306 |
|
|
autoimmune disease, susceptibility to, 6
|
13303.0 |
|
|
Cbl mutation-associated syndrome
|
13308 |
|
|
spinocerebellar ataxia type 10
|
11330 |
|
