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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:Fanconi renotubular syndrome 5
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Accession:DOID:0080761 term browser browse the term
Definition:A Fanconi syndrome that is characterized by proximal renotubular dysfunction from birth, followed by progressive kidney disease and pulmonary fibrosis and that has_material_basis_in homozygous mutation in the NDUFAF6 gene on chromosome 8q22. (DO)
Synonyms:exact_synonym: Acadian-variant Fanconi syndrome;   FRTS5
 primary_id: OMIM:618913
For additional species annotation, visit the Alliance of Genome Resources.

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Fanconi renotubular syndrome 5 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ndufaf6 NADH:ubiquinone oxidoreductase complex assembly factor 6 ISO ClinVar Annotator: match by term: FANCONI RENOTUBULAR SYNDROME 5 OMIM
PMID:27466185 NCBI chr 5:24,297,169...24,320,804
Ensembl chr 5:24,297,094...24,320,786
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16091
    syndrome 7036
      Fanconi syndrome 9
        Fanconi renotubular syndrome 5 1
Path 2
Term Annotations click to browse term
  disease 16091
    Developmental Diseases 9586
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 8437
        genetic disease 7958
          monogenic disease 5742
            autosomal genetic disease 4757
              autosomal recessive disease 2616
                Fanconi renotubular syndrome 5 1
paths to the root