ZFIN Human Disease: Perrault syndrome

OBO ID: DOID:0050857

Term Name:	Perrault syndrome		Search Ontology:
Synonyms:
Definition:	A syndrome that is characterized by sensorineural hearing loss and ovarian failure. (2)
References:	GARD:2542 OMIM:233400 OMIM:614129 OMIM:614926 OMIM:615300 OMIM:PS233400 ORDO:2855
Ontology:	Human Disease ( DOID:0050857 )

Relationships

is a type of:	autosomal recessive disease syndrome autosomal recessive disease syndrome Show first 5 Terms
has subtype:	Perrault syndrome 6 Perrault syndrome 6 Show first 5 Terms

OTHER Perrault syndrome PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CLPP	clpp	Perrault syndrome 3	614129
HARS	hars	Perrault syndrome 2	614926
HARS2	hars	Perrault syndrome 2	614926
HSD17B4	hsd17b4	Perrault syndrome 1	233400
LARS2	lars2	Perrault syndrome 4	615300

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None