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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:autosomal dominant keratosis follicularis spinulosa decalvans
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Accession:DOID:0080755 term browser browse the term
Definition:A keratosis follicularis spinulosa decalvans that has_material_basis_in autosomal dominant inheritance. (DO)
Synonyms:primary_id: MESH:C567553
 alt_id: OMIM:612843


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18976
    Pathological Conditions, Signs and Symptoms 13376
      Anatomical Pathological Conditions 2664
        alopecia 94
          autosomal dominant keratosis follicularis spinulosa decalvans 0
Path 2
Term Annotations click to browse term
  disease 18976
    disease of anatomical entity 18260
      nervous system disease 14116
        Neurologic Manifestations 10102
          sensory system disease 7022
            skin disease 4047
              keratosis 185
                ichthyosis 91
                  keratosis pilaris atrophicans 3
                    keratosis follicularis spinulosa decalvans 2
                      autosomal dominant keratosis follicularis spinulosa decalvans 0
paths to the root