Disease #05803 (CMS23 (myasthenic syndrome, congenital, type 23, presynaptic (CMS23)), OMIM:618197)

Global Variome shared LOVD

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

Official abbreviation	CMS23
Name	myasthenic syndrome, congenital, type 23, presynaptic (CMS23)
OMIM ID	618197
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SLC25A1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-08-05 11:55:28 +02:00 (CEST)
Date last edited	2020-08-05 11:55:59 +02:00 (CEST)

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