Disease #07244 (HPE10 (holoprosencephaly, type 10), OMIM:621143)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	HPE10
Name	holoprosencephaly, type 10
OMIM ID	621143
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DISP1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2026-03-10 17:37:26 +01:00 (CET)
Date last edited	N/A

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