|
lipodystrophy, familial partial, type 4
|
13478 |
|
|
lipodystrophy, familial partial, type 4; FPLD4
|
http://purl.obolibrary.org/obo/MONDO_0013478 |
|
|
nystagmus, infantile periodic alternating, x-linked
|
C564478 |
|
|
combined oxidative phosphorylation deficiency 29
|
14781 |
|
|
combined oxidative phosphorylation deficiency 29; COXPD29
|
14781 |
|
|
combined oxidative phosphorylation deficiency 36
|
54781 |
|
|
combined oxidative phosphorylation deficiency 36; COXPD36
|
http://purl.obolibrary.org/obo/MONDO_0054781 |
|
|
combined oxidative phosphorylation deficiency caused by mutation in TXN2
|
14781 |
|
|
combined oxidative phosphorylation deficiency type 29
|
14781 |
|
|
salmonella food poisoning
|
D012478 |
|
|
salmonella food poisonings
|
D012478 |
|
|
hemangioma, sclerosing, pulmonary
|
D047868 |
|
|
sclerosing hemangioma, pulmonary
|
D047868 |
|
|
sclerosing hemangiomas, pulmonary
|
D047868 |
|
