Format

Send to:

Choose Destination

RP32 retinitis pigmentosa 32 (autosomal recessive) [ Homo sapiens (human) ]

Gene ID: 641433, updated on 8-Apr-2017

Summary

Official Symbol
RP32provided by HGNC
Official Full Name
retinitis pigmentosa 32 (autosomal recessive)provided by HGNC
Primary source
HGNC:HGNC:21902
See related
MIM:609913
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Phenotypes

Associated conditions

Description Tests
retinitis pigmentosa 32 (autosomal recessive)
GeneReviews: Not available
Support Center