Disease #00049 (FAP2 (FAMILIAL ADENOMATOUS POLYPOSIS 2), OMIM:608456)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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Official abbreviation	FAP2
Name	FAMILIAL ADENOMATOUS POLYPOSIS 2
OMIM ID	608456
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MUTYH
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-03-03 14:10:12 +00:00 (UTC)
Date last edited	2023-06-16 09:42:25 +00:00 (UTC)