General Information of Disease (ID: DISTTXO6)

Disease Name Autosomal recessive nonsyndromic hearing loss 77
Synonyms
autosomal recessive deafness 77; deafness, autosomal recessive type 77; autosomal recessive nonsyndromic deafness caused by mutation in LOXHD1; LOXHD1 autosomal recessive nonsyndromic deafness; DFNB77; autosomal recessive nonsyndromic deafness 77; deafness, autosomal recessive 77; autosomal recessive nonsyndromic deafness type 77; autosomal recessive nonsyndromic hearing loss 77
Definition Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the LOXHD1 gene.
Disease Hierarchy
DIS8G9R9: Hearing loss, autosomal recessive
DISTTXO6: Autosomal recessive nonsyndromic hearing loss 77
Disease Identifiers
MONDO ID
MONDO_0013119
MESH ID
C567543
UMLS CUI
C2746083
OMIM ID
613079
MedGen ID
412541

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
LOXHD1 OTOJ2RHI Strong Autosomal recessive [1]
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References

1 [Sonographic differential diagnosis of gallbladder concretions]. Rofo. 1979 Jul;131(1):106-7. doi: 10.1055/s-0029-1231392.