Disease #04319 (CMS4B (myasthenic syndrome, congenital, type 4B, fast-channel (CMS-4B)), OMIM:616324)

Global Variome shared LOVD

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

Official abbreviation	CMS4B
Name	myasthenic syndrome, congenital, type 4B, fast-channel (CMS-4B)
OMIM ID	616324
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CHRNE
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-08-28 21:28:11 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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