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


RGD uses the Human Disease Ontology (DO, 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:infantile histiocytoid cardiomyopathy
go back to main search page
Accession:DOID:0080198 term browser browse the term
Definition:An intrinsic cardiomyopathy characterized by the presence of characteristic pale granular foamy histiocyte-like cells within the myocardium and has_material_basis_in a mutation in the gene encoding mitochondrial cytochrome b. (DO)
Synonyms:exact_synonym: foamy myocardial transformation of infancy;   focal lipid cardiomyopathy;   infantile xanthomatous cardiomyopathy;   oncocytic cardiomyopathy
 primary_id: MESH:C535584
 alt_id: OMIM:500000
 xref: GARD:9511
For additional species annotation, visit the Alliance of Genome Resources.

show annotations for term's descendants           Sort by:
infantile histiocytoid cardiomyopathy term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G FAM135A family with sequence similarity 135 member A ISO ClinVar Annotator: match by term: Infantile histiocytoid cardiomyopathy ClinVar NCBI chr 6:68,248,800...68,396,398
Ensembl chr 6:71,546,924...71,694,408
JBrowse link
G NDUFB11 NADH:ubiquinone oxidoreductase subunit B11 ISO ClinVar Annotator: match by term: Infantile histiocytoid cardiomyopathy ClinVar PMID:25741868, PMID:25772934 NCBI chr  X:39,579,460...39,582,462
Ensembl chr  X:47,437,573...47,440,578
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12751
    Developmental Diseases 9009
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7844
        genetic disease 7395
          monogenic disease 5466
            infantile histiocytoid cardiomyopathy 2
Path 2
Term Annotations click to browse term
  disease 12751
    disease of anatomical entity 12281
      cardiovascular system disease 3301
        heart disease 2338
          cardiomyopathy 966
            intrinsic cardiomyopathy 671
              infantile histiocytoid cardiomyopathy 2
paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.