Label | Id |
---|
trisomy 5p13 | 13169 | |
nephronophthisis (disease) caused by mutation in XPNPEP3 | 13163 | |
Parkinson disease 16 | 13167 | |
parkinson disease 16 | 13167 | |
Parkinson disease 16; PARK16 | http://purl.obolibrary.org/obo/MONDO_0013167 | |
nephronophthisis-like nephropathy 1; NPHPL1 | http://purl.obolibrary.org/obo/MONDO_0013163 | |
cardiomyopathy, dilated, 1DD | 13168 | |
dilated cardiomyopathy 1DD | 13168 | |
cardiomyopathy, dilated, 1DD; CMD1DD | http://purl.obolibrary.org/obo/MONDO_0013168 | |
gamma aminobutyric acid transaminase deficiency | 13166 | |
gamma-amino butyric acid transaminase deficiency | 13166 | |
cancer, spleen | D013160 | |
cancer, splenic | D013160 | |
cancers, spleen | D013160 | |
cancers, splenic | D013160 |