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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:Minimal Pigment Type Albinism
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Accession:DOID:9008042 term browser browse the term
Synonyms:exact_synonym: Oculocutaneous albinism, minimal pigment type
 primary_id: MESH:C537044
 alt_id: RDO:0002803
For additional species annotation, visit the Alliance of Genome Resources.


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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
        ocular albinism 9
          Minimal Pigment Type Albinism 0
Path 2
Term Annotations click to browse term
  disease 16122
    disease of anatomical entity 15369
      nervous system disease 10977
        sensory system disease 5248
          skin disease 2715
            pigmentation disease 217
              Hypopigmentation 105
                Albinism 47
                  ocular albinism 9
                    Minimal Pigment Type Albinism 0
paths to the root