|
hereditary iron-loading anemia
|
C536761 |
|
|
hereditary sideroblastic anemia
|
C536761 |
|
|
sideroblastic, x-linked anemia
|
C536761 |
|
|
neurodegeneration with brain iron accumulation 4
|
13674 |
|
|
neurodegeneration with brain iron accumulation 4; NBIA4
|
http://purl.obolibrary.org/obo/MONDO_0013674 |
|
|
neurodegeneration with brain iron accumulation caused by mutation in C19orf12
|
13674 |
|
|
neurodegeneration with brain iron accumulation due to C19orf12 mutation
|
13674 |
|
|
neurodegeneration with brain iron accumulation type 4
|
13674 |
|
|
charlevoix-saguenay spastic ataxia
|
C536787 |
|
|
axillary neoplasm, benign
|
36781 |
|
|
Wolfram-like syndrome, autosomal dominant
|
13673 |
|
|
WOLFRAM-like syndrome, autosomal dominant
|
http://purl.obolibrary.org/obo/MONDO_0013673 |
|
|
adenoid cystic carcinoma of pharynx
|
6367 |
|
|
WOLFRAM-like syndrome, autosomal dominant; WFSL
|
http://purl.obolibrary.org/obo/MONDO_0013673 |
|
