Disease #06825 (SMALED2B (spinal muscular atrophy, lower extremity-predominant, type 2B), OMIM:618291)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	SMALED2B
Name	spinal muscular atrophy, lower extremity-predominant, type 2B
OMIM ID	618291
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	BICD2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	2022-12-22 17:13:53 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.