Disease #04436 (MDDGA9 (dystrophy-dystroglycanopathy, muscular, (congenital with brain and eye anomalies), type A9), OMIM:616538)

Official abbreviation MDDGA9
Name dystrophy-dystroglycanopathy, muscular, (congenital with brain and eye anomalies), type A9
OMIM ID 616538
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene DAG1
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2024-01-12 21:35:59 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00104053 - - - - - - - - - - - MDDGA9 - POMGNT2 POMGNT2 2 1 Céline Bouchet Seraphin
00472249 - Verebi et al. (submitted) - F - France - - - - - MDDGA9 0012531 : Pain, 0003326 : Myalgia - DAG1 1 1 Camille Verebi
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