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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:GSD IV, Neuromuscular Form, Fatal Perinatal
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Accession:DOID:9006655 term browser browse the term
Synonyms:primary_id: MESH:C565541;   RDO:0014149



show annotations for term's descendants           Sort by:
GSD IV, Neuromuscular Form, Fatal Perinatal term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Gbe1 1,4-alpha-glucan branching enzyme 1 ISO DNA:missense mutations, nonsense mutation, splice site mutation:exons, intron: multiple
ClinVar Annotator: match by term: Gsd IV, neuromuscular form, fatal perinatal
ClinVar
RGD
PMID:8247964 PMID:10384399 PMID:15452297 PMID:16199547 PMID:20058079 More... RGD:18337290 NCBI chr11:8,734,806...9,000,226
Ensembl chr11:8,734,820...9,000,210
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21128
    disease of anatomical entity 18212
      musculoskeletal system disease 8271
        neuromuscular disease 3051
          GSD IV, Neuromuscular Form, Fatal Perinatal 1
Path 2
Term Annotations click to browse term
  disease 21128
    Developmental Disease 18448
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 18308
        genetic disease 18252
          inherited metabolic disorder 6212
            carbohydrate metabolic disorder 3265
              glycogen metabolism disorder 264
                glycogen storage disease 264
                  glycogen storage disease IV 4
                    GSD IV, Neuromuscular Form, Fatal Perinatal 1
paths to the root