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Perrault Syndrome

Disease ID: disease_node_20349

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Dbxref	GARD:2542, MIM:233400, MIM:614129, MIM:614926, MIM:615300, MIM:PS233400, ORDO:2855
Subclassof	DOID_225, DOID_0050737
Data Source	DOID
Doid Label	Perrault syndrome
Doid Description	A syndrome that is characterized by sensorineural hearing loss and ovarian failure.
Has Material Basis In	GENO_0000148
Disease Node Id	disease_node_20349
Doid Id	DOID_0050857
Label	Perrault Syndrome

Outgoing r'ship SUBCLASS_OF to/from Syndrome(ID:disease_node_7213) (Disease)
Incoming r'ship SUBCLASS_OF to/from Perrault Syndrome 6(ID:disease_node_20350) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)

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