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ONTOLOGY REPORT - ANNOTATIONS


Term:Congenital Cataracts, Facial Dysmorphism, and Neuropathy
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Accession:DOID:9005826 term browser browse the term
Synonyms:exact_synonym: CCFDN;   Cataract, Congenital, With Facial Dysmorphism And Neuropathy
 primary_id: MESH:C565822;   RDO:0014360
 alt_id: OMIM:604168
For additional species annotation, visit the Alliance of Genome Resources.


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Congenital Cataracts, Facial Dysmorphism, and Neuropathy term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ctdp1 CTD phosphatase subunit 1 JBrowse link 18 76,922,913 76,985,095 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14096
      nervous system disease 9148
        Congenital Cataracts, Facial Dysmorphism, and Neuropathy 1
Path 2
Term Annotations click to browse term
  disease 14926
    disease of anatomical entity 14096
      nervous system disease 9148
        sensory system disease 4270
          eye and adnexa disease 1996
            eye disease 1996
              lens disease 191
                cataract 184
                  Congenital Cataracts, Facial Dysmorphism, and Neuropathy 1
paths to the root

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