Disease #00226 (POH (heteroplasia, osseous, progressive (POH)), OMIM:166350)

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	Curator: Johan T. den Dunnen

Official abbreviation	POH
Name	heteroplasia, osseous, progressive (POH)
OMIM ID	166350
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GNAS
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-10-09 19:15:39 +02:00 (CEST)
Date last edited	N/A