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ONTOLOGY REPORT - ANNOTATIONS


Term:Macular Dystrophy, Retinal, 1, North Carolina Type
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Accession:DOID:9001226 term browser browse the term
Synonyms:exact_synonym: CAPED;   MCDR1;   NCMD;   North Carolina macular dystrophy;   central areolar pigment epithelial dystrophy;   central retinal pigment epithelial dystrophy;   progressive foveal dystrophy
 primary_id: MESH:C537835
 alt_id: OMIM:136550
For additional species annotation, visit the Alliance of Genome Resources.


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12016
    sensory system disease 4262
      eye and adnexa disease 2041
        eye disease 2041
          corneal disease 168
            corneal dystrophy 41
              Macular Dystrophy, Retinal, 1, North Carolina Type 0
Path 2
Term Annotations click to browse term
  disease 12016
    disease of anatomical entity 11623
      nervous system disease 9286
        sensory system disease 4262
          eye and adnexa disease 2041
            eye disease 2041
              Hereditary Eye Diseases 497
                corneal dystrophy 41
                  Macular Dystrophy, Retinal, 1, North Carolina Type 0
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.