Disease #05770 (KLEFS2 (syndrome, Kleefstra, type 2 (KLEFS2)), OMIM:617768)

Official abbreviation KLEFS2
Name syndrome, Kleefstra, type 2 (KLEFS2)
OMIM ID 617768
Human Phenotype Ontology Project (HPO) HPO
Inheritance AD
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MLL3
Associated tissues -
Disease features -
Remarks -