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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:achromatopsia 7
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Accession:DOID:0110009 term browser browse the term
Definition:An autosomal recessive disorder resulting from lack of cone photoreceptor function. Affected individuals present from birth or early infancy with photophobia, nystagmus, severely reduced visual acuity, and color blindness. (OMIM)
Synonyms:exact_synonym: ACHM7
 primary_id: OMIM:616517
 alt_id: RDO:9001328
For additional species annotation, visit the Alliance of Genome Resources.


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achromatopsia 7 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Atf6 activating transcription factor 6 ISO ClinVar Annotator: match by term: Achromatopsia 7 OMIM
ClinVar
PMID:24824130 PMID:26029869 PMID:26063662 NCBI chr13:89,053,457...89,242,531
Ensembl chr13:89,055,983...89,242,443
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16122
    sensory system disease 5248
      eye disease 2673
        blindness 93
          color blindness 10
            achromatopsia 7
              achromatopsia 7 1
Path 2
Term Annotations click to browse term
  disease 16122
    disease of anatomical entity 15369
      nervous system disease 10977
        sensory system disease 5248
          eye disease 2673
            Vision Disorders 158
              blindness 93
                color blindness 10
                  achromatopsia 7
                    achromatopsia 7 1
paths to the root