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ONTOLOGY REPORT - ANNOTATIONS


Term:amelogenesis imperfecta hypomaturation type 2A5
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Accession:DOID:0110063 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: AI2A5;   amelogenesis imperfecta type IIA5;   amelogenesis imperfecta, hypomaturation type, IIA5
 primary_id: OMIM:615887
 alt_id: RDO:9001335
For additional species annotation, visit the Alliance of Genome Resources.


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amelogenesis imperfecta hypomaturation type 2A5 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Slc24a4 solute carrier family 24 member 4 JBrowse link 6 126,015,799 126,158,727 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15603
    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 2A5 1
Path 2
Term Annotations click to browse term
  disease 15603
    disease of anatomical entity 14934
      nervous system disease 10239
        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 2A5 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.