Disease #05386 (CSS5 (syndrome, Coffin-Siris, type 5 (CSS5)), OMIM:616938)

Official abbreviation CSS5
Name syndrome, Coffin-Siris, type 5 (CSS5)
OMIM ID 616938
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene SMARCE1
Associated tissues -
Disease features autosomal dominant
Remarks -