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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:Ullrich congenital muscular dystrophy 1B
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Accession:DOID:0060942 term browser browse the term
Definition:An Ullrich congenital muscular dystrophy characterized by generalized muscle weakness and striking hypermobility of distal joints in conjunction with variable contractures of more proximal joints and normal intelligence that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the COL6A2 gene on chromosome 21q22. (DO)
Synonyms:exact_synonym: UCMD1B
 related_synonym: UCMD1A/1B, DIGENIC;   ULLRICH CONGENITAL MUSCULAR DYSTROPHY 1A/1B, DIGENIC
 alt_id: DOID:9005971
 xref: MIM:620727;   MONDO:0958235



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Path 1
Term Annotations click to browse term
  disease 15834
    Pathological Conditions, Signs and Symptoms 12336
      Pathologic Processes 7774
        Sclerosis 21
          Ullrich congenital muscular dystrophy 11
            Ullrich congenital muscular dystrophy 1B 1
Path 2
Term Annotations click to browse term
  disease 15834
    disease of anatomical entity 15490
      nervous system disease 13586
        peripheral nervous system disease 4302
          neuropathy 4114
            neuromuscular disease 3186
              muscular disease 2198
                muscle tissue disease 1335
                  atrophic muscular disease 673
                    Brody myopathy 669
                      muscular dystrophy 654
                        congenital muscular dystrophy 217
                          Collagen VI-related Myopathy 68
                            Ullrich congenital muscular dystrophy 11
                              Ullrich congenital muscular dystrophy 1B 1
paths to the root