Disease #03817 (MDDGA10 (dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A10 (MDDGA-10)), OMIM:615041)

Official abbreviation MDDGA10
Name dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A10 (MDDGA-10)
OMIM ID 615041
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TMEM5
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.