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
skeletal dysplasia, mental retardation syndrome hirsutism C536705
wiedemann oldigs oppermann syndrome C536705
curatolo cilio pessagno syndrome C536701
wieacker wolff syndrome C536703
deafness, autosomal recessive 116 33670
mental retardation, x-linked, with congenital contractures and low fingertip arches C536703
myopia, high, with cataract and vitreoretinal degeneration 13670
myopia, high, with cataract and vitreoretinal degeneration; MCVD http://purl.obolibrary.org/obo/MONDO_0013670