Details of Disease | DrugMAP

General Information of Disease (ID: DIST8JV7)

Disease Name	Hearing loss, autosomal recessive 107
Synonyms	deafness, autosomal recessive 107; autosomal recessive nonsyndromic deafness 107; DFNB107
Disease Hierarchy	DIS8G9R9: Hearing loss, autosomal recessive DIST8JV7: Hearing loss, autosomal recessive 107
Disease Identifiers	MONDO ID MONDO_0033199 UMLS CUI C4539964 OMIM ID 617639 MedGen ID 1622558

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
WBP2	OTBZR5JS	Moderate	Autosomal recessive	[1]
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References

1	Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearing. EMBO Mol Med. 2016 Mar 1;8(3):191-207. doi: 10.15252/emmm.201505523.