Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

Dyschromatosis universalis hereditaria

Hearing impairment

A decreased magnitude of the sensory perception of sound.

Total: 0

(per page)

PMID (PMCID)