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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:autosomal recessive limb-girdle muscular dystrophy type 2X
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Accession:DOID:0110290 term browser browse the term
Definition:An autosomal recessive muscle disorder characterized by slowly progressive onset of proximal lower limb weakness in adulthood. Affected individuals also develop cardiac arrhythmias resulting in syncopal episodes as young adults or later in life. LGMD2X is caused by homozygous mutation in the BVES gene on chromosome 6q21. (OMIM)
Synonyms:exact_synonym: CARDIAC ARRHYTHMIA WITH INCREASED SERUM CREATINE KINASE;   CARICK;   LGMD2X;   LGMDR25;   MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 25;   muscular dystrophy, limb-girdle, type 2X
 primary_id: OMIM:616812
 alt_id: RDO:9001160
 xref: ORDO:476084
For additional species annotation, visit the Alliance of Genome Resources.


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autosomal recessive limb-girdle muscular dystrophy type 2X term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G BVES blood vessel epicardial substance ISO OMIM NCBI chr12:62,542,274...62,581,110
Ensembl chr12:62,545,666...62,579,548
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12678
    Pathological Conditions, Signs and Symptoms 7610
      Pathologic Processes 5602
        Cardiac Arrhythmias 584
          autosomal recessive limb-girdle muscular dystrophy type 2X 1
Path 2
Term Annotations click to browse term
  disease 12678
    disease of anatomical entity 12216
      nervous system disease 9976
        peripheral nervous system disease 2371
          neuropathy 2214
            neuromuscular disease 1713
              muscular disease 1157
                muscle tissue disease 784
                  atrophic muscular disease 311
                    muscular dystrophy 309
                      limb-girdle muscular dystrophy 143
                        autosomal recessive limb-girdle muscular dystrophy 103
                          autosomal recessive limb-girdle muscular dystrophy type 2X 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.