autosomal recessive nonsyndromic deafness 67

Summary

DOID:0110518 - autosomal recessive nonsyndromic deafness 67

Disease Ontology Definition: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 LHFPL5 gene on chromosome 6p21.

Synonyms: DFNB67, autosomal recessive deafness 67,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: lhfpl5

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012460 - autosomal recessive nonsyndromic hearing loss 67

MONDO:0012460 - autosomal recessive nonsyndromic hearing loss 67

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive nonsyndromic deafness (is_a)