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
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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

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Path 1
Term Annotations click to browse term
  disease 14920
    Stomatognathic Diseases 853
      tooth disease 228
        teeth hard tissue disease 38
          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 14920
    disease of anatomical entity 14086
      nervous system disease 9150
        sensory system disease 4265
          mouth disease 665
            tooth disease 228
              Tooth Abnormalities 106
                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.