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Autosomal-Mitochondrial Sensorineural Deafness

Disease ID: disease_node_17739

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Dbxref	MIM:221745
Subclassof	DOID_10003, DOID_0080578
Data Source	DOID
Doid Label	autosomal-mitochondrial sensorineural deafness
Doid Description	A sensorineural hearing loss characterized by progressive, severe to profound deafness that has_material_basis_in digenic inheritance of mutations in the mitochondrial gene MTRNR1 and an unidentified nuclear gene.
Has Material Basis In	GENO_0000930
Disease Node Id	disease_node_17739
Doid Id	DOID_0111752
Label	Autosomal-Mitochondrial Sensorineural Deafness

Outgoing r'ship SUBCLASS_OF to/from Hearing Loss, Sensorineural(ID:disease_node_3710) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Digenic Disease(ID:disease_node_13627) (Disease)

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