Disease #05797 (CSS11 (Coffin-Siris syndrome, type 11 (CSS11)), OMIM:618779)

Official abbreviation CSS11
Name Coffin-Siris syndrome, type 11 (CSS11)
OMIM ID 618779
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SMARCD1
Associated tissues -
Disease features -
Remarks -
Date created 2020-07-25 09:07:00 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00472232 - Verebi et al. (submitted) - F - France - - - - - CSS11 Metabolic myopathy - SMARCD1 1 3 Camille Verebi
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