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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:Bethlem Myopathy 2
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Accession:DOID:9006278 term browser browse the term
Synonyms:exact_synonym: BTHLM2
 primary_id: OMIM:616471
 alt_id: RDO:9001375
For additional species annotation, visit the Alliance of Genome Resources.


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Bethlem Myopathy 2 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G COL12A1 collagen type XII alpha 1 chain ISO OMIM NCBI chr 1:90,744,409...90,875,127
Ensembl chr 1:90,744,429...90,875,118
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12693
    physical disorder 2359
      congenital muscular dystrophy 70
        Bethlem myopathy 8
          Bethlem Myopathy 2 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
                        Bethlem myopathy 8
                          Bethlem Myopathy 2 1
paths to the root