ONTOLOGY REPORT - ANNOTATIONS


Term:amelogenesis imperfecta hypomaturation type 2A4
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Accession:DOID:0110062 term browser browse the term
Definition:An amelogenesis imperfecta caused by homozygous mutation in the C4ORF26 gene on chromosome 4q21. (DO)
Synonyms:exact_synonym: AI2A4;   amelogenesis imperfecta type IIA4;   amelogenesis imperfecta, hypomaturation type IIA4
 primary_id: OMIM:614832
 alt_id: RDO:9000167
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amelogenesis imperfecta hypomaturation type 2A4 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Odaph odontogenesis associated phosphoprotein JBrowse link 14 17,575,295 17,583,214 RGD:7240710
RGD:8554872

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Path 1
Term Annotations click to browse term
  disease 14823
    Stomatognathic Diseases 845
      tooth disease 223
        teeth hard tissue disease 36
          dental enamel hypoplasia 30
            amelogenesis imperfecta 28
              Amelogenesis Imperfecta Hypomaturation Type 6
                amelogenesis imperfecta hypomaturation type 2A4 1
Path 2
Term Annotations click to browse term
  disease 14823
    disease of anatomical entity 13997
      nervous system disease 9111
        sensory system disease 4244
          mouth disease 658
            tooth disease 223
              Tooth Abnormalities 103
                dental enamel hypoplasia 30
                  amelogenesis imperfecta 28
                    Amelogenesis Imperfecta Hypomaturation Type 6
                      amelogenesis imperfecta hypomaturation type 2A4 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.