Disease #07019 (ALS28 (sclerosis, lateral, amyotrophic), OMIM:620452)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	ALS28
Name	sclerosis, lateral, amyotrophic
OMIM ID	620452
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LRP12
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-08-16 12:08:52 +02:00 (CEST)
Date last edited	N/A

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