Disease #05798 (MGORS7 (syndrome, Meier-Gorlin, type 7 (MGORS7)), OMIM:617063)

Official abbreviation MGORS7
Name syndrome, Meier-Gorlin, type 7 (MGORS7)
OMIM ID 617063
Human Phenotype Ontology Project (HPO) HPO
Inheritance AR
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CDC45
Associated tissues -
Disease features -
Remarks -