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Summary Literature (0)
DOID:0050857 - Perrault syndrome

Disease Ontology Definition:A syndrome that is characterized by sensorineural hearing loss and ovarian failure.

Synonyms:

Xenbase Genes : lars2, clpp, twnk, hsd17b4, eral1, hars2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0017312 - Perrault syndrome


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), syndrome (is_a)