Disease #00187 (PBT (PIEBALD TRAIT), OMIM:172800)

Official abbreviation PBT
Name PIEBALD TRAIT
OMIM ID 172800
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene KIT
Associated tissues -
Disease features -
Remarks -
Date created 2023-07-17 12:06:47 +00:00 (UTC)
Date last edited N/A

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