PubDictionaries

MONDO_bioport_pref_name

183,974 entries

Label	Id

Feingold syndrome caused by mutation in MYCN	8115
main bronchus cancer	2811
autosomal dominant cerebellar ataxia type I caused by mutation in ATXN1	8119
autosomal recessive cerebellar ataxia-saccadic intrusion syndrome	11811
high altitude cerebral edema	21811
trisomy 6p chromosome 6	C537811
complex cardiac defects, and splenic defects, X-linked situs inversus	C538116
cancer, sigmoid colon	D012811
neoplasm, sigmoid colon	D012811
neoplasms, sigmoid colon	D012811
situs inversus, complex cardiac defects, and splenic defects, X-linked	C538116
night blindness, congenital stationary, type1i	32811
simple chronic conjunctivitis	4811
vitamin e deficiencies	D014811
microcephaly and digital abnormalities with Normal intelligence	http://purl.obolibrary.org/obo/MONDO_0008115