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ONTOLOGY REPORT - ANNOTATIONS


Term:amelogenesis imperfecta type 3A
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Accession:DOID:0110055 term browser browse the term
Definition:An amelogenesis imperfecta that has_material_basis_in heterozygous mutation in the FAM83H gene. (DO)
Synonyms:exact_synonym: ADHCAI;   AI3A;   amelogenesis imperfecta hypomineralization type;   amelogenesis imperfecta type IIIA;   amelogenesis imperfecta, hypocalcification type, autosomal dominant
 primary_id: MESH:C562880
 alt_id: OMIM:130900
For additional species annotation, visit the Alliance of Genome Resources.


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amelogenesis imperfecta type 3A term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fam83h family with sequence similarity 83, member H JBrowse link 7 117,062,748 117,070,936 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16022
    Stomatognathic Diseases 931
      tooth disease 272
        teeth hard tissue disease 62
          dental enamel hypoplasia 54
            amelogenesis imperfecta 52
              amelogenesis imperfecta type 3 3
                amelogenesis imperfecta type 3A 1
Path 2
Term Annotations click to browse term
  disease 16022
    disease of anatomical entity 15275
      nervous system disease 10770
        sensory system disease 4976
          mouth disease 720
            tooth disease 272
              Tooth Abnormalities 141
                dental enamel hypoplasia 54
                  amelogenesis imperfecta 52
                    amelogenesis imperfecta type 3 3
                      amelogenesis imperfecta type 3A 1
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