Search Ontology:
Human Disease

autosomal-mitochondrial sensorineural deafness

Term ID
DOID:0111752
Synonyms
Definition
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. (2)
References
Ontology
Human Disease   ( DOID:0111752 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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