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DOID:0110521 - autosomal recessive nonsyndromic deafness 70
Disease Ontology Definition:An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the PNPT1 gene on chromosome 2p16.
Synonyms: DFNB70, autosomal recessive deafness 70,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MIM:614934 - deafness, autosomal recessive 70; dfnb70 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee