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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 1
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Accession:DOID:9001544 term browser browse the term
Synonyms:exact_synonym: MDDGB1;   MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 1;   congenital muscular dystrophy, POMT1-related;   congenital muscular dystrophy-dystroglycanopathy with impaired intellectual development, type B1;   muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual impairment), type B, 1
 primary_id: OMIM:613155
For additional species annotation, visit the Alliance of Genome Resources.


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Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 1 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G POMT1 protein O-mannosyltransferase 1 ISO OMIM NCBI chr 1:271,432,196...271,448,584
Ensembl chr 1:271,432,210...271,451,080
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12693
    Developmental Diseases 8990
      Neurodevelopmental Disorders 4417
        intellectual disability 2136
          Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 1 1
Path 2
Term Annotations click to browse term
  disease 12693
    disease of anatomical entity 12233
      nervous system disease 9973
        peripheral nervous system disease 2315
          neuropathy 2154
            neuromuscular disease 1698
              muscular disease 1116
                muscle tissue disease 750
                  atrophic muscular disease 293
                    muscular dystrophy 291
                      congenital muscular dystrophy 70
                        muscular dystrophy-dystroglycanopathy 37
                          Muscular Dystrophy-Dystroglycanopathy (congenital with mental retardation), Type B, 1 1
paths to the root