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ONTOLOGY REPORT - ANNOTATIONS


Term:amelogenesis imperfecta hypomaturation type 2A3
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Accession:DOID:0110061 term browser browse the term
Definition:An amelogenesis imperfecta caused by homozygous mutation in the WDR72 gene. (DO)
Synonyms:exact_synonym: Ai2a3;   amelogenesis imperfecta hypomaturation type IIA3;   amelogenesis imperfecta type IIA3
 primary_id: MESH:C567706
 alt_id: OMIM:613211;   RDO:0015702
For additional species annotation, visit the Alliance of Genome Resources.


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amelogenesis imperfecta hypomaturation type 2A3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Wdr72 WD repeat domain 72 JBrowse link 8 80,965,734 81,125,710 RGD:7240710
RGD:8554872

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 2A3 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 2A3 1
paths to the root

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