Disease #02194 (ALS15 (sclerosis, lateral, amyotrophic, type 15, with/without frontotemporal dementia (ALS15)), OMIM:300857)

Official abbreviation ALS15
Name sclerosis, lateral, amyotrophic, type 15, with/without frontotemporal dementia (ALS15)
OMIM ID 300857
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene UBQLN2
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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