Disease #00415 (PCT (porphyria cutanea tarda (PCT)), OMIM:176100)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	PCT
Name	porphyria cutanea tarda (PCT)
OMIM ID	176100
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	HFE, UROD
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-06-15 21:27:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.