Label | Id |
---|
carcinoma in situ of oropharynx | 21298 | |
carcinoma in situ of the oropharynx | 21298 | |
glomangioma of skin | 2298 | |
zone of skin glomangioma | 2298 | |
SLC4A1 hereditary spherocytosis | 12981 | |
EPB42 hereditary spherocytosis | 12985 | |
disorder of stomach | 4298 | |
fracture, hip, susceptibility to | 5298 | |
congenital nonprogressive spinocerebellar ataxia | 7298 | |
cantu craniofaciofrontodigital syndrome | C567298 | |
oropharyngeal cancer stage 0 | 21298 | |
valvular aortic stenosis | 42981 | |
Lesch Nyhan syndrome | 10298 | |
GATA2 deficiency/MonoMac syndrome | http://purl.obolibrary.org/obo/MONDO_0042982 | |
17q21.31 microduplication syndrome | 13298 |