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

Dyschromatosis symmetrica hereditaria

A rare genodermatosis characterised by the presence of hyperpigmented and hypopigmented macules, principally located on the extremities and limbs.

Aortic valve calcification

Deposition of calcium salts in the aortic valve.

Total: 0

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PMID (PMCID)