Disease #05852 (MDDGB15 (dystrophy, muscular, dystroglycanopathy (congenital with impaired intellectual development), type B15 (MDDGB15)), OMIM:618992)

Official abbreviation	MDDGB15
Name	dystrophy, muscular, dystroglycanopathy (congenital with impaired intellectual development), type B15 (MDDGB15)
OMIM ID	618992
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DPM3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-10-10 20:00:57 +02:00 (CEST)
Date last edited	N/A

Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.

Global Variome shared LOVD