Hereditary disorder of tooth   1148766007

SNOMED CT code


SNOMED code1148766007
nameHereditary disorder of tooth
statusactive
date introduced2021-07-31
fully specified name(s)Hereditary disorder of tooth (disorder)
synonymsHereditary disorder of tooth
attributes - group1
Finding siteTooth structure   38199008
parents
children
  • 4H leukodystrophy   1208933000
  • Ackerman syndrome   722280000
  • ADULT (acro-dermato-ungual-lacrimal-tooth) syndrome   720464003
  • Amelogenesis imperfecta   78494001
  • Anterior maxillary protrusion, strabismus, intellectual disability syndrome   1222706005
  • Arthrogryposis and ectodermal dysplasia syndrome   786039009
  • Autosomal dominant hypohidrotic ectodermal dysplasia syndrome   7731005
  • Autosomal recessive hypohidrotic ectodermal dysplasia syndrome   27025001
  • Book syndrome   722296002
  • Cerebellar-facial-dental syndrome   1237475006
  • Cleidocranial dysostosis   65976001
  • Conductive deafness, ptosis, skeletal anomalies syndrome   763213001
  • Congenital deafness with labyrinthine aplasia, microtia and microdontia   702360007
  • Contracture with ectodermal dysplasia and orofacial cleft syndrome   720746006
  • Craniosynostosis and dental anomalies syndrome   773332008
  • Curly hair, acral keratoderma, caries syndrome   763686007
  • Curry-Hall syndrome   277807007
  • Deafness, enamel hypoplasia, nail defect syndrome   721085000
  • Dentin dysplasia   109492001
  • Dentinogenesis imperfecta   196286005
  • Dermatoosteolysis Kirghizian type   721090002
  • Dermo-odonto dysplasia   721091003
  • Developmental absence of tooth   234951001
  • Ectodermal dysplasia syndactyly syndrome   771335004
  • Ectodermal dysplasia trichoodontoonychial type   734018003
  • Ectodermal dysplasia with blindness syndrome   721208007
  • Erythrokeratodermia cardiomyopathy syndrome   1179293006
  • GAPO syndrome   721843003
  • Haim Munk syndrome   719973009
  • Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome   773553003
  • Hypohidrotic X-linked ectodermal dysplasia   239007005
  • Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome   763658004
  • Incontinentia pigmenti syndrome   367520004
  • Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome   764995008
  • Nance-Horan syndrome   445257004
  • Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome   723442008
  • Oculocerebrodental syndrome   1255268002
  • Oculoosteocutaneous syndrome   722061006
  • Oculotrichodysplasia   722062004
  • Odonto-tricho-ungual-digito-palmar syndrome   722063009
  • Odontotrichomelic syndrome   239028001
  • Otodental syndrome   1237343009
  • Pilodental dysplasia, refractive errors syndrome   771240009
  • Postaxial polydactyly, dental, vertebral anomalies syndrome   773279006
  • Primary failure of tooth eruption   1231153007
  • Schinzel-Giedion syndrome   18899000
  • Schmitt Gillenwater Kelly syndrome   716092007
  • Steatocystoma multiplex with natal tooth syndrome   719306007
  • Stern Lubinsky Durrie syndrome   723584003
  • Steroid dehydrogenase deficiency and dental anomaly syndrome   723583009
  • Teebi Shaltout syndrome   771265006
  • Temtamy preaxial brachydactyly syndrome   777998000
  • Trichoodontoonychial dysplasia   766813000
  • Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome   719910004
  • XTE syndrome   7037003
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Disorder of digestive system   53619000
        Disorder of digestive organ   76712006
          Tooth disorder   234947003
            Hereditary disorder of tooth   1148766007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Digestive system finding   386617003
      Disorder of digestive system   53619000
        Digestive system hereditary disorder   363080007
          Hereditary disorder of tooth   1148766007

ancestors
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