Disease #01439 (HPE2 (holoprosencephaly, type 2 (HPE-2)), OMIM:157170)

Official abbreviation HPE2
Name holoprosencephaly, type 2 (HPE-2)
OMIM ID 157170
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene SIX3
Associated tissues -
Disease features -
Remarks -