Disease #03185 (CCDS (deficiency, cerebral creatine, syndrome (CCDS)))

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

	Curator: Global Variome, with Curator vacancy

Official abbreviation	CCDS
Name	deficiency, cerebral creatine, syndrome (CCDS)
OMIM ID	-
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 3 genes	GAMT, GATM, SLC6A8
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-05-07 10:08:15 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.