ONTOLOGY REPORT - ANNOTATIONS


Term:Chromosome 2q37 Deletion Syndrome
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Accession:DOID:9001256 term browser browse the term
Synonyms:exact_synonym: 2q37 deletion syndrome;   Albright hereditary osteodystrophy-like syndrome;   BDMR;   Brachydactyly-Mental Retardation syndrome;   Chromosome 2, monosomy 2q37;   Deletion 2q37;   Monosomy 2q37
 primary_id: MESH:C538317;   RDO:0004279
 alt_id: OMIM:600430;   RDO:0002493
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Chromosome 2q37 Deletion Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Farp2 FERM, ARH/RhoGEF and pleckstrin domain protein 2 JBrowse link 9 100,660,366 100,767,940 RGD:11554173
G Hdac4 histone deacetylase 4 JBrowse link 9 99,052,945 99,299,715 RGD:8554872
RGD:7240710
RGD:11554173
G Hdlbp high density lipoprotein binding protein JBrowse link 9 100,554,574 100,624,707 RGD:11554173
G Pask PAS domain containing serine/threonine kinase JBrowse link 9 100,450,595 100,479,719 RGD:11554173

Term paths to the root
Path 1
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  disease 14875
    syndrome 4220
      Chromosome 2q37 Deletion Syndrome 4
Path 2
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  disease 14875
    Pathological Conditions, Signs and Symptoms 7362
      Pathologic Processes 4865
        Chromosome Aberrations 519
          Aneuploidy 426
            Monosomy 381
              Chromosome Deletion 381
                Chromosome 2q37 Deletion Syndrome 4
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.