Disease #01087 (MDDGB3 (dystrophy-dystroglycanopathy, muscular, (congenital with mental retardation), type B3), OMIM:613151)

Official abbreviation MDDGB3
Name dystrophy-dystroglycanopathy, muscular, (congenital with mental retardation), type B3
OMIM ID 613151
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene POMGNT1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2024-01-12 21:39:15 +01:00 (CET)

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