Disease #00006 (PCTT (PANCREATITIS, HEREDITARY), OMIM:167800)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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Official abbreviation	PCTT
Name	PANCREATITIS, HEREDITARY
OMIM ID	167800
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	PRSS1, SPINK1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2016-07-08 13:43:37 +00:00 (UTC)
Date last edited	2023-06-16 09:57:10 +00:00 (UTC)