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USH1H Usher syndrome 1H (autosomal recessive) [ Homo sapiens (human) ]

Gene ID: 100271837, updated on 8-Apr-2017

Summary

Official Symbol
USH1Hprovided by HGNC
Official Full Name
Usher syndrome 1H (autosomal recessive)provided by HGNC
Primary source
HGNC:HGNC:22433
See related
MIM:612632
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Bibliography

Related articles in PubMed

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

Phenotypes

Associated conditions

Description Tests
Usher syndrome 1H (autosomal recessive)
GeneReviews: Not available
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