ONTOLOGY REPORT - ANNOTATIONS


Term:dental enamel hypoplasia
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Accession:DOID:693 term browser browse the term
Definition:An acquired or hereditary condition due to deficiency in the formation of tooth enamel (AMELOGENESIS). It is usually characterized by defective, thin, or malformed DENTAL ENAMEL. Risk factors for enamel hypoplasia include gene mutations, nutritional deficiencies, diseases, and environmental factors.
Synonyms:exact_synonym: Enamel Ageneses;   Enamel Agenesis;   Enamel Hypoplasia;   Enamel Hypoplasias;   Hypoplastic Enamel;   Molar Incisor Hypomineralization
 primary_id: MESH:D003744;   RDO:0002164
For additional species annotation, visit the Alliance of Genome Resources.


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amelogenesis imperfecta term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Amelx amelogenin, X-linked JBrowse link X 26,439,197 26,450,495 RGD:1300370
G Dlx3 distal-less homeobox 3 JBrowse link 10 82,937,971 82,943,367 RGD:8554872
G Enam enamelin JBrowse link 14 21,194,635 21,219,529 RGD:11554173
G Fam20c FAM20C, golgi associated secretory pathway kinase JBrowse link 12 17,913,771 17,972,733 RGD:11560487
RGD:11560491
G Fam83h family with sequence similarity 83, member H JBrowse link 7 117,062,748 117,070,936 RGD:11554173
G Gpr68 G protein-coupled receptor 68 JBrowse link 6 124,874,151 124,903,949 RGD:8554872
G Ltbp3 latent transforming growth factor beta binding protein 3 JBrowse link 1 221,099,155 221,116,096 RGD:11554173
G Wdr72 WD repeat domain 72 JBrowse link 8 80,965,734 81,125,710 RGD:8554872
amelogenesis imperfecta hypomaturation type 2A2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mmp20 matrix metallopeptidase 20 JBrowse link 8 5,823,147 5,875,555 RGD:7240710
RGD:8554872
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
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
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
Amelogenesis Imperfecta Hypomaturation Type, 2A6 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Gpr68 G protein-coupled receptor 68 JBrowse link 6 124,874,151 124,903,949 RGD:8554872
RGD:7240710
amelogenesis imperfecta type 1A term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Lamb3 laminin subunit beta 3 JBrowse link 13 112,031,614 112,073,187 RGD:7240710
RGD:8554872
amelogenesis imperfecta type 1B term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dlx3 distal-less homeobox 3 JBrowse link 10 82,937,971 82,943,367 RGD:8554872
G Enam enamelin JBrowse link 14 21,194,635 21,219,529 RGD:1598908
RGD:8554872
RGD:7240710
amelogenesis imperfecta type 1C term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Enam enamelin JBrowse link 14 21,194,635 21,219,529 RGD:7240710
RGD:8554872
G Mmp20 matrix metallopeptidase 20 JBrowse link 8 5,823,147 5,875,555 RGD:8554872
G Wdr72 WD repeat domain 72 JBrowse link 8 80,965,734 81,125,710 RGD:8554872
amelogenesis imperfecta type 1E term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Amelx amelogenin, X-linked JBrowse link X 26,439,197 26,450,495 RGD:7240710
RGD:8554872
G Arhgap6 Rho GTPase activating protein 6 JBrowse link X 26,314,561 26,845,242 RGD:8554872
amelogenesis imperfecta type 1F term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ambn ameloblastin JBrowse link 14 21,239,887 21,252,534 RGD:7240710
RGD:8554872
amelogenesis imperfecta type 1G term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fam20a FAM20A, golgi associated secretory pathway pseudokinase JBrowse link 10 97,962,467 98,017,171 RGD:7240710
RGD:8554872
G Prkar1a protein kinase cAMP-dependent type I regulatory subunit alpha JBrowse link 10 97,940,705 97,959,199 RGD:8554872
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
Amelogenesis Imperfecta Type 1J term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Acp4 acid phosphatase 4 JBrowse link 1 100,226,311 100,234,536 RGD:8554872
RGD:7240710
amelogenesis imperfecta type 2A1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Klk4 kallikrein-related peptidase 4 JBrowse link 1 99,828,944 99,834,642 RGD:8554872
RGD:7240710
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
amelogenesis imperfecta type 3B term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Amtn amelotin JBrowse link 14 21,282,488 21,301,966 RGD:7240710
Amelogenesis Imperfecta Type 3C term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Relt RELT, TNF receptor JBrowse link 1 165,884,407 165,902,022 RGD:7240710
amelogenesis imperfecta type 4 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dlx3 distal-less homeobox 3 JBrowse link 10 82,937,971 82,943,367 RGD:7240710
RGD:8554872
brachyolmia-amelogenesis imperfecta syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ltbp3 latent transforming growth factor beta binding protein 3 JBrowse link 1 221,099,155 221,116,096 RGD:7240710
RGD:8554872
Burnett Schwartz Berberian Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Lrp1 LDL receptor related protein 1 JBrowse link 7 70,846,313 70,927,028 RGD:8554872
Cone Rod Dystrophy Amelogenesis Imperfecta term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cnnm4 cyclin and CBS domain divalent metal cation transport mediator 4 JBrowse link 9 43,049,587 43,088,690 RGD:8554872
Deafness Enamel Hypoplasia Nail Defects term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Gatad1 GATA zinc finger domain containing 1 JBrowse link 4 27,647,005 27,658,533 RGD:8554872
G Pex1 peroxisomal biogenesis factor 1 JBrowse link 4 27,659,376 27,698,037 RGD:8554872
RGD:7240710
G Pex6 peroxisomal biogenesis factor 6 JBrowse link 9 16,568,743 16,580,900 RGD:11554173
Jalili Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Chst5 carbohydrate sulfotransferase 5 JBrowse link 19 44,115,065 44,136,092 RGD:7240710
KERATOSIS PILARIS ATROPHICANS term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Lrp1 LDL receptor related protein 1 JBrowse link 7 70,846,313 70,927,028 RGD:7240710
Kohlschutter Tonz Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rogdi rogdi atypical leucine zipper JBrowse link 10 10,761,477 10,766,096 RGD:7240710
RGD:8554872
Short Stature, Amelogenesis Imperfecta, and Skeletal Dysplasia with Scoliosis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Slc10a7 solute carrier family 10, member 7 JBrowse link 19 32,857,984 33,081,359 RGD:7240710
Singleton Merten Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ifih1 interferon induced with helicase C domain 1 JBrowse link 3 48,557,696 48,604,097 RGD:8554872
RGD:11554173
Singleton-Merten Syndrome 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ifih1 interferon induced with helicase C domain 1 JBrowse link 3 48,557,696 48,604,097 RGD:7240710
RGD:8554872
Singleton-Merten Syndrome 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ddx58 DEXD/H-box helicase 58 JBrowse link 5 56,486,584 56,536,898 RGD:8554872
RGD:7240710
Tricho-Dento-Osseous Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dlx3 distal-less homeobox 3 JBrowse link 10 82,937,971 82,943,367 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14919
    Stomatognathic Diseases 853
      tooth disease 227
        teeth hard tissue disease 38
          dental enamel hypoplasia 32
            Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus 0
            Ameloonychohypohidrotic Syndrome 0
            Enamel Hypoplasia, Cataracts, and Aqueductal Stenosis 0
            Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia 0
            Oculodentoosseous Dysplasia Recessive 0
            Pfeiffer Palm Teller Syndrome 0
            Seow Najjar Syndrome 0
            Singleton Merten Syndrome + 2
            Tricho-Dento-Osseous Syndrome 1
            Trichoodontoonychial Dysplasia 0
            amelogenesis imperfecta + 30
Path 2
Term Annotations click to browse term
  disease 14919
    disease of anatomical entity 14083
      nervous system disease 9147
        sensory system disease 4264
          mouth disease 665
            tooth disease 227
              Tooth Abnormalities 105
                dental enamel hypoplasia 32
                  Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus 0
                  Ameloonychohypohidrotic Syndrome 0
                  Enamel Hypoplasia, Cataracts, and Aqueductal Stenosis 0
                  Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia 0
                  Oculodentoosseous Dysplasia Recessive 0
                  Pfeiffer Palm Teller Syndrome 0
                  Seow Najjar Syndrome 0
                  Singleton Merten Syndrome + 2
                  Tricho-Dento-Osseous Syndrome 1
                  Trichoodontoonychial Dysplasia 0
                  amelogenesis imperfecta + 30
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.