Genetic disorder of nail   402775007

SNOMED CT code


SNOMED code402775007
nameGenetic disorder of nail
statusactive
date introduced2003-07-31
fully specified name(s)Genetic disorder of nail (disorder)
synonymsGenetic disorder of nail
attributes - group1
Finding siteNail unit structure   770802007
parents
children
  • ADULT (acro-dermato-ungual-lacrimal-tooth) syndrome   720464003
  • Alopecia, onychodysplasia, hypohidrosis, deafness ectodermal dysplasia   239010003
  • Anonychia with microcephaly syndrome   720494009
  • Arthrogryposis and ectodermal dysplasia syndrome   786039009
  • Autosomal dominant hypohidrotic ectodermal dysplasia syndrome   7731005
  • Autosomal recessive hypohidrotic ectodermal dysplasia syndrome   27025001
  • Autosomal recessive nail dysplasia   782878007
  • Brachymorphism with onychodysplasia and dysphalangism syndrome   720573009
  • Congenital isolated onychodysplasia   1254893000
  • Cooks syndrome   720747002
  • Curly hair, acral keratoderma, caries syndrome   763686007
  • Curry-Hall syndrome   277807007
  • Deafness with onychodystrophy syndrome   773735007
  • Deafness, enamel hypoplasia, nail defect syndrome   721085000
  • Dermatoosteolysis Kirghizian type   721090002
  • Dermo-odonto dysplasia   721091003
  • Dystrophic epidermolysis bullosa nails only   722436002
  • Ectodermal dysplasia trichoodontoonychial type   734018003
  • Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome   1279835008
  • Hereditary clubbing   239055005
  • Hereditary distal onycholysis   1254945005
  • Hereditary lymphedema and yellow nails   400211001
  • Hereditary striate leuconychia   278523002
  • Hidrotic ectodermal dysplasia Christianson Fourie type   771239007
  • Hidrotic ectodermal dysplasia Halal type   721147000
  • Hidrotic ectodermal dysplasia syndrome   54209007
  • Hirschsprung disease with nail hypoplasia and dysmorphism   721223002
  • Hypodontia and nail dysgenesis   239021007
  • Hypohidrotic X-linked ectodermal dysplasia   239007005
  • Hypotrichosis and deafness syndrome   783555001
  • Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome   763658004
  • Incontinentia pigmenti syndrome   367520004
  • Inherited deformity of nail   402776008
  • Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome   1271009
  • Leukonychia totalis, acanthosis-nigricans-like lesions, abnormal hair syndrome   773700005
  • Mammary digital nail syndrome   718679004
  • Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome   764995008
  • Nail dystrophy due to Darier's disease   403788000
  • Nail-patella syndrome   22199006
  • Oculotrichodysplasia   722062004
  • Odontotrichomelic syndrome   239028001
  • Oto-onycho-peroneal syndrome   441944007
  • Pachydermoperiostosis syndrome   88220006
  • Pachyonychia congenita syndrome   39427000
  • Pigmentation defects, palmoplantar keratoderma, skin carcinoma syndrome   1230005002
  • Pili torti onychodysplasia syndrome   723451000
  • PLACK syndrome   1237509001
  • Schinzel-Giedion syndrome   18899000
  • Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome   720345008
  • Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome   773625007
  • Split-foot malformation, mesoaxial polydactyly syndrome   1172635005
  • Stern Lubinsky Durrie syndrome   723584003
  • Temple Baraitser syndrome   725140007
  • Trichoodontoonychial dysplasia   766813000
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of limb structure   302293008
      Nail finding   247480006
        Disorder of nail   17790008
          Genetic disorder of nail   402775007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Genetic disorder of nail   402775007

ancestors
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