Disease #02654 (LIS-1 (lissencephaly, type 1 (LIS-1)), OMIM:607432)

Official abbreviation LIS-1
Name lissencephaly, type 1 (LIS-1)
OMIM ID 607432
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PAFAH1B1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A