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

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CSS5
Name	Coffin-Siris syndrome, type 5 (CSS5)
OMIM ID	616938
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SMARCE1
Associated tissues	-
Disease features	autosomal dominant
Remarks	-
Date created	2018-02-01 14:01:46 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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