ONTOLOGY REPORT - ANNOTATIONS


Term:hypotrichosis 8
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Accession:DOID:0110705 term browser browse the term
Definition:A hypotrichosis has_material_basis_in a autosomal recessive mutation of LPAR6 on chromosome 13q14.2. (DO)
Synonyms:exact_synonym: HYPT8;   LAH3;   hypotrichosis, localized, autosomal recessive 3
 primary_id: MESH:C566950
 alt_id: RDO:0015155
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hypotrichosis 8 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Krt25 keratin 25 JBrowse link 11 99,315,516 99,322,941 RGD:8554872
G Lpar6 lysophosphatidic acid receptor 6 JBrowse link 14 73,237,891 73,240,358 RGD:8554872
RGD:13592920
G Rb1 RB transcriptional corepressor 1 JBrowse link 14 73,194,453 73,325,885 RGD:8554872

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  disease 11829
    Developmental Diseases 7517
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 6836
        genetic disease 6166
          hypotrichosis 8 3
Path 2
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  disease 11829
    disease of anatomical entity 11278
      nervous system disease 8560
        sensory system disease 4037
          skin disease 2128
            hair disease 212
              hypotrichosis 96
                hypotrichosis 8 3
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.