Disease #00438 (HPE (holoprosencephaly (HPE)), OMIM:236100)

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Official abbreviation	HPE
Name	holoprosencephaly (HPE)
OMIM ID	236100
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 5 genes	GLI2, SHH, SIX3, TGIF1, ZIC2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-06-30 10:33:45 +02:00 (CEST)
Date last edited	N/A