Disease #07012 (LGMDR28;MYPLG (dystrophy, muscular, limb-girdle, autosomal recessive, type 28 (MYPLG)), OMIM:620375)

Global Variome shared LOVD

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

Official abbreviation	LGMDR28;MYPLG
Name	dystrophy, muscular, limb-girdle, autosomal recessive, type 28 (MYPLG)
OMIM ID	620375
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HMGCR
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-06-02 10:39:26 +02:00 (CEST)
Date last edited	2024-01-12 21:14:20 +01:00 (CET)

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