Disease #01506 (PBT (Piebald trait (PBT)), OMIM:172800)

Official abbreviation PBT
Name Piebald trait (PBT)
OMIM ID 172800
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 2 genes KIT, SNAI2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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