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Human Disease

autosomal recessive nonsyndromic deafness 98

Term ID
DOID:0110540
Synonyms
  • autosomal recessive deafness 98
  • DFNB98
Definition
An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TSPEAR gene on chromosome 21q22. https://www.ncbi.nlm.nih.gov/pubmed/22678063
References
Ontology
Human Disease   ( DOID:0110540 )
Relationships
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Genes Involved
Zebrafish Models
Citations