|
spinocerebellar ataxia, autosomal recessive 25; SCAR25
|
http://purl.obolibrary.org/obo/MONDO_0033115 |
|
|
spinocerebellar ataxia, autosomal recessive 26
|
33116 |
|
|
spinocerebellar ataxia, autosomal recessive 26; SCAR26
|
http://purl.obolibrary.org/obo/MONDO_0033116 |
|
|
early repolarization associated with ventricular fibrillation
|
13318 |
|
|
t cell-negative, b cell-negative, NK cell-positive SCID
|
C563311 |
|
|
transient monocular blindness
|
43310 |
|
|
large intestine carcinoma
|
24331 |
|
|
genetic transient congenital hypothyroidism
|
44331 |
|
|
retinitis pigmentosa caused by mutation in ARL6
|
13312 |
|
|
retinitis pigmentosa caused by mutation in IMPG2
|
13314 |
|
