Disease #04292 (MDDGA12 (dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A12 (MDDGA-12)), OMIM:615249)

Official abbreviation MDDGA12
Name dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A12 (MDDGA-12)
OMIM ID 615249
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 POMK
Associated tissues -
Disease features -
Remarks -
Date created 2015-06-19 22:43:00 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00081036 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MDDGA12 Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12 (OMIM:615249) POMK POMK 1 1 Daniel Trujillano
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