Disease #00728 (MGORS-5 (Meier-Gorlin syndrome, type 5 (MGORS-5)), OMIM:613805)

Official abbreviation MGORS-5
Name Meier-Gorlin syndrome, type 5 (MGORS-5)
OMIM ID 613805
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CDC6
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A