Disease #03738 (MDDGA8 (dystrophy-dystroglycanopathy, muscular, congenital with brain and eye anomalies), type A8), OMIM:614830)

Official abbreviation MDDGA8
Name dystrophy-dystroglycanopathy, muscular, congenital with brain and eye anomalies), type A8
OMIM ID 614830
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene POMGNT2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2024-01-12 21:18:14 +01:00 (CET)


Individuals

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00080890 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MDDGA8 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 8 (OMIM:614830) POMGNT2 POMGNT2 1 1 Daniel Trujillano
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