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ONTOLOGY REPORT - ANNOTATIONS


Term:Amelogenesis Imperfecta Hypomaturation Type, 2A6
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Accession:DOID:9006208 term browser browse the term
Definition:Autosomal recessive amelogenesis imperfecta of the pigmented hypomaturation type characterized by slightly soft enamel of normal thickness that is hypomineralized and detaches easily from the dentin. (OMIM)
Synonyms:exact_synonym: AI2A6;   Amelogenesis Imperfecta, Hypomaturation Type, IIA6
 primary_id: OMIM:617217
 alt_id: RDO:9001336
For additional species annotation, visit the Alliance of Genome Resources.


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Amelogenesis Imperfecta Hypomaturation Type, 2A6 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Gpr68 G protein-coupled receptor 68 JBrowse link 6 124,874,151 124,903,949 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15639
    Stomatognathic Diseases 870
      tooth disease 241
        teeth hard tissue disease 40
          dental enamel hypoplasia 32
            amelogenesis imperfecta 30
              Amelogenesis Imperfecta Hypomaturation Type 6
                Amelogenesis Imperfecta Hypomaturation Type, 2A6 1
Path 2
Term Annotations click to browse term
  disease 15639
    disease of anatomical entity 14969
      nervous system disease 10242
        sensory system disease 4697
          mouth disease 680
            tooth disease 241
              Tooth Abnormalities 112
                dental enamel hypoplasia 32
                  amelogenesis imperfecta 30
                    Amelogenesis Imperfecta Hypomaturation Type 6
                      Amelogenesis Imperfecta Hypomaturation Type, 2A6 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.