Disease #01517 (POREN-1 (porencephaly, type 1 (POREN-1)), OMIM:175780)

Official abbreviation POREN-1
Name porencephaly, type 1 (POREN-1)
OMIM ID 175780
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene COL4A1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A