oculopharyngodistal myopathy; OPDM
|
http://purl.obolibrary.org/obo/MONDO_0008117 |
|
benign prostatic Hypertrophy
|
10811 |
|
primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma
|
15811 |
|
spinocerebellar ataxia autosomal recessive 4
|
11811 |
|
spinocerebellar ataxia, autosomal recessive 4
|
11811 |
|
spinocerebellar ataxia, autosomal recessive 4; SCAR4
|
http://purl.obolibrary.org/obo/MONDO_0011811 |
|
autosomal dominant cerebellar ataxia type I caused by mutation in ATXN1
|
8119 |
|
malignant main bronchus neoplasm
|
2811 |
|
prostatic hyperplasia, benign
|
10811 |
|
prostatic hyperplasia, benign; BPH
|
http://purl.obolibrary.org/obo/MONDO_0010811 |
|
aneurysm, intracranial berry, 8
|
12811 |
|
Feingold syndrome caused by mutation in MYCN
|
8115 |
|