Disease #06998 (ALS26 (sclerosis, lateral, amyotrophic, with/without frontotemporal dementia, type 26), OMIM:619133)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	ALS26
Name	sclerosis, lateral, amyotrophic, with/without frontotemporal dementia, type 26
OMIM ID	619133
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TIA1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-01-21 16:45:54 +01:00 (CET)
Date last edited	N/A

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