Disease #01101 (MDDGB1 (dystrophy-dystroglycanopathy, muscular, (congenital with mental retardation), type B1), OMIM:613155)

Official abbreviation MDDGB1
Name dystrophy-dystroglycanopathy, muscular, (congenital with mental retardation), type B1
OMIM ID 613155
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 POMT1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2024-01-12 21:48:57 +01:00 (CET)


Individuals

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00080974 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MDDGB1 Muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 1 (OMIM:613155) POMT1 POMT1 1 1 Daniel Trujillano
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