ZFIN Human Disease: nonsyndromic deafness

OBO ID: DOID:0050563

Term Name:	nonsyndromic deafness		Search Ontology:
Synonyms:	nonsyndromic hearing loss nonsyndromic hereditary hearing loss
Definition:	An auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms. (3)
References:	MESH:C580334
Ontology:	Human Disease ( DOID:0050563 )

Relationships

is a type of:	auditory system disease auditory system disease Show first 5 Terms
has subtype:	autosomal dominant nonsyndromic deafness autosomal recessive nonsyndromic deafness drug-induced hearing loss X-linked nonsyndromic deafness Y-linked deafness autosomal dominant nonsyndromic deafness autosomal recessive nonsyndromic deafness drug-induced hearing loss X-linked nonsyndromic deafness Y-linked deafness Show first 5 Terms

OTHER nonsyndromic deafness PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS

Fish	Conditions	Citations
WT + MO5-lrp5 + MO6-lrp5	standard conditions	Xia et al., 2017

PHENOTYPE No data available

CITATIONS (14)