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ONTOLOGY REPORT - ANNOTATIONS


Term:amelogenesis imperfecta type 1H
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Accession:DOID:0110064 term browser browse the term
Definition:An autosomal recessive amelogenesis imperfecta characterized by hypoplastic and hypomineralized tooth enamel that may be rough, pitted, and/or discolored. (OMIM)
Synonyms:exact_synonym: AI1H;   amelogenesis imperfecta type IH
 primary_id: OMIM:616221
 alt_id: RDO:9001338
For additional species annotation, visit the Alliance of Genome Resources.


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amelogenesis imperfecta type 1H term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Itgb6 integrin subunit beta 6 JBrowse link 3 46,652,624 46,775,362 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15590
    Stomatognathic Diseases 867
      tooth disease 238
        teeth hard tissue disease 38
          dental enamel hypoplasia 32
            amelogenesis imperfecta 30
              amelogenesis imperfecta type 1H 1
Path 2
Term Annotations click to browse term
  disease 15590
    disease of anatomical entity 14919
      nervous system disease 10196
        sensory system disease 4659
          mouth disease 678
            tooth disease 238
              Tooth Abnormalities 112
                dental enamel hypoplasia 32
                  amelogenesis imperfecta 30
                    amelogenesis imperfecta type 1H 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.