Disease #00756 (CSS3;MRD15 (syndrome, Coffin-Siris, type 3 (CSS3, mental retardation, autosomal dominant, type 15 (MRD15))), OMIM:614608)

Official abbreviation CSS3;MRD15
Name syndrome, Coffin-Siris, type 3 (CSS3, mental retardation, autosomal dominant, type 15 (MRD15))
OMIM ID 614608
Human Phenotype Ontology Project (HPO) HPO
Inheritance AD
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene SMARCB1
Associated tissues -
Disease features -
Remarks -