Disease #01368 (HPE-3 (holoprosencephaly, type 3 (HPE-3)), OMIM:142945)

Official abbreviation HPE-3
Name holoprosencephaly, type 3 (HPE-3)
OMIM ID 142945
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene SHH
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A