Disease #03585 (HPE-11 (holoprosencephaly, type 11 (HPE-11)), OMIM:614226)

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Official abbreviation	HPE-11
Name	holoprosencephaly, type 11 (HPE-11)
OMIM ID	614226
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CDON
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A