Disease #00115 (HPE7 (HOLOPROSENCEPHALY 7), OMIM:610828)

Official abbreviation HPE7
Name HOLOPROSENCEPHALY 7
OMIM ID 610828
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PTCH1
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-16 09:59:39 +00:00 (UTC)
Date last edited N/A

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