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Disease Ontology Term: autosomal recessive nonsyndromic deafness 21

DO ID
DOID:0110479
Description
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the TECTA gene on chromosome 11q23.3.
Synonyms
autosomal recessive deafness 21, DFNB21
View DO Annotations for yeast and other model organisms at the Alliance of Genome Resources

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Annotations

Manually Curated

There are no manually curated annotations for autosomal recessive nonsyndromic deafness 21.

High-throughput

There are no high-throughput annotations for autosomal recessive nonsyndromic deafness 21.

Computational

There are no computational annotations for autosomal recessive nonsyndromic deafness 21.
monogenic disease (0)