Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
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Preferred Name

CEREBELLAR HYPOPLASIA
ID

http://purl.bioontology.org/ontology/OMIM/213000
cui

C0266470
MIMTYPEMEANING

Mendelian phenotype or locus, molecular basis unknown.
notation

213000
OMIM Entry Type

5
OMIM MimType Value

perc
prefLabel

CEREBELLAR HYPOPLASIA
tui

T019
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http://purl.obolibrary.org/obo/DOID_0070338 Human Disease Ontology 123 LOOM
http://purl.bioontology.org/ontology/MESH/C562568 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C562568 Medical Subject Headings LOOM