Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

ONTOLOGY REPORT - ANNOTATIONS


Term:hypotrichosis 13
go back to main search page
Accession:DOID:0110710 term browser browse the term
Definition:A hypotrichosis that has_material_basis_in a autosomal dominant mutation of KRT71 on chromosome 12q13.13. (DO)
Synonyms:exact_synonym: HYPT13;   hypotrichosis with woolly hair
 primary_id: OMIM:615896
 alt_id: RDO:9001603
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 
hypotrichosis 13 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Krt71 keratin 71 JBrowse link 7 143,345,201 143,371,346 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14924
    Developmental Diseases 7770
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7092
        genetic disease 6457
          hypotrichosis 13 1
Path 2
Term Annotations click to browse term
  disease 14924
    disease of anatomical entity 14094
      nervous system disease 9141
        sensory system disease 4249
          skin disease 2260
            hair disease 224
              hypotrichosis 108
                hypotrichosis 13 1
paths to the root

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.