|
Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2V
|
14665 |
|
|
Charcot-Marie-Tooth disease, axonal, type 2V
|
14665 |
|
|
deficiency of biotinidase
|
9665 |
|
|
Charcot-Marie-Tooth disease, axonal, type 2V; CMT2V
|
http://purl.obolibrary.org/obo/MONDO_0014665 |
|
|
early-onset non-syndromic cataract caused by mutation in BFSP1
|
12665 |
|
|
Charcot-Marie-Tooth disease caused by mutation in NAGLU
|
14665 |
|
|
cytosolic phosphoenolpyruvate carboxykinase deficiency
|
C536654 |
|
|
juvenile-onset multiple carboxylase deficiency
|
9665 |
|
|
late-onset multiple carboxylase deficiency
|
9665 |
|
|
cervical endometrioid carcinoma
|
3665 |
|
|
cervix endometrioid carcinoma
|
3665 |
|
|
amyloid angiopathy, cerebral
|
D016657 |
|
|
nodular sclerosis classical Hodgkin lymphoma
|
4665 |
|
|
dystonia, primary cervical
|
C566572 |
|
