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)

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