ONTOLOGY REPORT - ANNOTATIONS


Term:hypotrichosis 3
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Accession:DOID:0110700 term browser browse the term
Definition:A hypotrichosis that has_material_basis_in a autosomal dominant mutation of KRT74 on chromosome 12q13.13. (DO)
Synonyms:exact_synonym: HTSS2;   HYPOTRICHOSIS SIMPLEX OF THE SCALP 2;   HYPT3
 primary_id: OMIM:613981
 alt_id: RDO:9000471
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Path 1
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  disease 14926
    Developmental Diseases 7774
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7096
        genetic disease 6457
          hypotrichosis 3 0
Path 2
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14092
      nervous system disease 9154
        sensory system disease 4267
          skin disease 2270
            hair disease 214
              hypotrichosis 98
                hypotrichosis 3 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.