Disease #02985 (HPE-7 (holoprosencephaly, type 7 (HPE-7)), OMIM:610828)

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	Curator: Johan T. den Dunnen

Official abbreviation	HPE-7
Name	holoprosencephaly, type 7 (HPE-7)
OMIM ID	610828
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PTCH1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A