dyschromatosis symmetrica hereditaria
pigmentation disease characterized by progressively pigmented and depigmented macules, often mixed in a reticulate pattern, concentrated on the dorsal extremities
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dyschromatosis symmetrica hereditaria
Summary
dyschromatosis symmetrica hereditaria is a rare disease[1].
Key Facts
- dyschromatosis symmetrica hereditaria's instance of is recorded as rare disease[2].
- dyschromatosis symmetrica hereditaria's instance of is recorded as class of disease[3].
- dyschromatosis symmetrica hereditaria is a type of pigmentation disorder[4].
- dyschromatosis symmetrica hereditaria is a type of hyperpigmentation of the skin[5].
- dyschromatosis symmetrica hereditaria's NCI Thesaurus ID is recorded as C118435[6].
- dyschromatosis symmetrica hereditaria's genetic association is recorded as ADAR[7].
- dyschromatosis symmetrica hereditaria's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060257[8].
- dyschromatosis symmetrica hereditaria's exact match is recorded as http://identifiers.org/doid/DOID:0060257[9].
- dyschromatosis symmetrica hereditaria's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_41[10].
- dyschromatosis symmetrica hereditaria's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].