ciliopathy
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http://purl.obolibrary.org/obo/DOID_0060340
A genetic disease associated with mutations encoding defective proteins, which result in either abnormal function formation or function of cilia.
Term info
Label
ciliopathy
Subsets
DO_MGI_slim
created by
emitraka
creation date
2015-05-21T10:41:29Z
has obo namespace
disease_ontology
id
DOID:0060340
imported from
http://purl.obolibrary.org/obo/doid.owl