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DOID:0050565 - autosomal recessive nonsyndromic deafness
Disease Ontology Definition:A nonsyndromic deafness characterized by an autosomal recessive inheritance mode.
Synonyms:
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0019588 - hearing loss, autosomal recessive |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee