MONDO_merge Find_IDs Find_Terms Annotation
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created at 2021-12-22 03:08:20 UTC
updated at 2021-12-22 07:06:09 UTC
MONDO_bioport_pref_name
183,974 entries
Label
Id
COXPD9 13811
herrmann syndrome C538113
X-linked laterality C538116
visceral heterotaxia C538116
capdepont teeth D003811
dentin, opalescent D003811
teeth, capdepont D003811
shields type 2 dentinogenesis imperfecta D003811
heterotaxy, visceral, 1, x-linked C538116
situs inversus, complex cardiac defects, and splenic defects, X-linked C538116
human herpesvirus 6 encephalitis C538117
visceral, 5, autosomal heterotaxy C538116
shields type II dentinogenesis imperfecta D003811
complex cardiac defects, and splenic defects, X-linked situs inversus C538116
ovarian mixed epithelial neoplasm 3811