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ONTOLOGY REPORT - ANNOTATIONS


Term:Y-linked monogenic disease
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Accession:DOID:0050738 term browser browse the term
Definition:Genetic diseases that are linked to mutant ALLELES on the Y CHROMOSOME in humans (Y CHROMOSOME, HUMAN) or the Y chromosome in other species. Included here are animal models of human Y-linked diseases.
Synonyms:exact_synonym: Genetic Diseases, Y Chromosome Linked;   Y-Linked Genetic Disease;   Y-linked disease
 primary_id: MESH:D050174
 alt_id: RDO:0003454
For additional species annotation, visit the Alliance of Genome Resources.


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Y-linked spermatogenic failure 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Kdm5d lysine demethylase 5D JBrowse link Y 501,058 589,267 RGD:11554173
G Rps4y2 ribosomal protein S4, Y-linked 2 JBrowse link 4 182,745,448 182,746,381 RGD:11554173
G Usp9y ubiquitin specific peptidase 9, Y-linked JBrowse link Y 1,260,512 1,403,417 RGD:8554872
RGD:7240710

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  disease 15626
    Developmental Diseases 8759
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7543
        genetic disease 7038
          monogenic disease 4659
            Y-linked monogenic disease 3
              Hairy Ears, Y-Linked 0
              Hodgkin Disease, Y-Linked Pseudoautosomal 0
              Y-Linked Deafness + 0
              Y-linked spermatogenic failure 1 0
              Y-linked spermatogenic failure 2 3
              retinitis pigmentosa Y-linked 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.