Disease #00045 (PJS (PEUTZ-JEGHERS SYNDROME), OMIM:175200)

MVZ für Humangenetik Regensburg

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Official abbreviation	PJS
Name	PEUTZ-JEGHERS SYNDROME
OMIM ID	175200
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	STK11
Associated tissues	-
Disease features	-
Remarks	-
Date created	2019-02-21 10:55:45 +00:00 (UTC)
Date last edited	2023-06-16 10:13:04 +00:00 (UTC)