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bn:03291493n
Noun Concept
Categories: Amino acid metabolism disorders, Autosomal dominant disorders, Disturbances of pigmentation, Disturbances of human pigmentation
EN
piebaldism  Partial albinism  PBT  PIEBALD TRAIT  PIEBALD TRAIT; PBT
EN
Piebaldism refers to the absence of mature melanin-forming cells in certain areas of the skin and hair. Wikipedia
Definitions
Relations
Sources
EN
Piebaldism refers to the absence of mature melanin-forming cells in certain areas of the skin and hair. Wikipedia
A pigmentation disorder in humans Wikipedia Disambiguation
Human disease Wikidata
A rare autosomal dominant disorder of melanocyte development, whose common characteristics include a congenital white forelock, scattered normally-pigmented and hyperpigmented macules, and a triangular depigmented patch on the forehead. Wiktionary
IS A
rare disease
leukoderma
HAS KIND
Ermine phenotype
GENETIC ASSOCIATION
SNAI2
KIT
HEALTH SPECIALTY
endocrinology
Wikipedia
EN
piebaldism
Wikidata
EN
piebaldism
Wiktionary
EN
piebaldism
Wikidata Alias
EN
Partial albinism, PBT, PIEBALD TRAIT, PIEBALD TRAIT; PBT, Piebaldism

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