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

Global Variome shared LOVD

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Official abbreviation	FTDALS2
Name	dementia, frontotemporal, and/or amyotrophic lateral sclerosis, type 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	2026-04-01 11:03:00 +02:00 (CEST)

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