Definition

An autosomal recessive nonsyndromic deafness characterized by early-onset, moderate to severe sensorineural hearing loss with no vestibular involvement that has_material_basis_in homozygous or compound heterozygous mutation in the MPZL2 gene on chromosome 11q23.33.

Synonyms

autosomal recessive deafness 111
DFNB111

Cross References

MIM:618145

Parent Terms

autosomal recessive nonsyndromic deafness

Child Terms

None

Sources of Associations

Associated Genes

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Associated Alleles

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Associated Models

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autosomal recessive nonsyndromic deafness 111

autosomal recessive nonsyndromic deafness 111

Associated Genes

Associated Alleles

Associated Models