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Echinobase
Summary Literature (0)
DOID:0050857 - Perrault syndrome

Disease Ontology Definition:An autosomal recessive disesase that is characterized by sensorineural hearing loss and ovarian failure.

Synonyms:

Echinobase Genes : clpp, lars2


OMIM:
MIM:614129 - perrault syndrome 3; prlts3
MIM:614926 - perrault syndrome 2; prlts2
MIM:615300 - perrault syndrome 4; prlts4

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

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