Disease #04130 (FTDALS2 (dementia, frontotemporal, and/or amyotrophic lateral sclerosis, type 2 (FTDALS-2)), OMIM:615911)

Official abbreviation	FTDALS2
Name	dementia, frontotemporal, and/or amyotrophic lateral sclerosis, type 2 (FTDALS-2)
OMIM ID	615911
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CHCHD10
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +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.

Global Variome shared LOVD