autosomal recessive nonsyndromic deafness 120 Disease Ontology Browser

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Disease Ontology Browser

autosomal recessive nonsyndromic deafness 120 (DOID:0070674)
Alliance: disease page
Synonyms: DFNB120
Alt IDs: OMIM:620238
Definition: An autosomal recessive nonsyndromic deafness characterized by congenital or prelingual onset of severe to profound sensorineural hearing loss that has_material_basis_in homozygous mutation in the MINAR2 gene on chromosome 5q23.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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