Details of Disease

General Information of Disease (ID: DISPP7H7)

Disease Name Hearing loss, autosomal recessive 110
Synonyms deafness, autosomal recessive 110; DFNB110
Disease Hierarchy
DIS8G9R9: Hearing loss, autosomal recessive
DISPP7H7: Hearing loss, autosomal recessive 110
Disease Identifiers
MONDO ID
MONDO_0054860
UMLS CUI
C4748162
OMIM ID
618094
MedGen ID
1648377

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
COCH OTBEHD89 Strong Autosomal recessive [1]
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References

1 Hearing and vestibular deficits in the Coch(-/-) null mouse model: comparison to the Coch(G88E/G88E) mouse and to DFNA9 hearing and balance disorder. Hear Res. 2011 Feb;272(1-2):42-8. doi: 10.1016/j.heares.2010.11.002. Epub 2010 Nov 10.