Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

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:myofibrillar myopathy 8
go back to main search page
Accession:DOID:0080308 term browser browse the term
Definition:A myofibrillar myopathy that is characterized by childhood onset of slowly progressive proximal muscle weakness and atrophy resulting in increased falls, gait problems, and difficulty running or climbing stairs, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the PYROXD1 gene on chromosome 12p12. (DO)
Synonyms:exact_synonym: MFM8
 primary_id: OMIM:617258
For additional species annotation, visit the Alliance of Genome Resources.



show annotations for term's descendants           Sort by:
 
myofibrillar myopathy 8 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Pyroxd1 pyridine nucleotide-disulphide oxidoreductase domain 1 ISO ClinVar Annotator: match by term: Myofibrillar myopathy 8 OMIM
ClinVar
PMID:25741868 PMID:27745833 PMID:28492532 PMID:30345904 PMID:31455395 More... NCBI chr 4:175,292,124...175,311,143
Ensembl chr 4:175,292,177...175,308,689
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18145
    physical disorder 4121
      congenital structural myopathy 170
        myofibrillar myopathy 63
          myofibrillar myopathy 8 1
Path 2
Term Annotations click to browse term
  disease 18145
    disease of anatomical entity 17519
      nervous system disease 13182
        peripheral nervous system disease 2997
          neuropathy 2785
            neuromuscular disease 2204
              muscular disease 1434
                muscle tissue disease 951
                  myopathy 782
                    congenital structural myopathy 170
                      myofibrillar myopathy 63
                        myofibrillar myopathy 8 1
paths to the root