SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease   32895009

SNOMED CT code


SNOMED code32895009
nameHereditary disease
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary disease (disorder)
synonyms
  • Hereditary disease
  • Inherited disease
parentsGenetic disease   782964007
children
  • Autosomal hereditary disorder   1899006
  • Blepharonasofacial malformation syndrome   717913006
  • Chronic granulomatous disease   387759001
  • Citrullinemia   398680004
  • Connective tissue hereditary disorder   363045008
  • Craniodigital syndrome and intellectual disability syndrome   763665007
  • Developmental hereditary disorder   363070008
  • Familial benign copper deficiency   763531001
  • Familial hemorrhagic diathesis   6935003
  • Familial thyroglossal duct cyst   717331000
  • Fetus with hereditary disease   199531009
  • Genetic syndrome   290028006  removed: 2019-07-31
  • Growth delay due to insulin-like growth factor I resistance   715625007
  • Hereditary amyloidosis   367601000119103
  • Hereditary ataxia   763597000
  • Hereditary cancer-predisposing syndrome   699346009
  • Hereditary coagulation factor deficiency   16922007
  • Hereditary disease in family possibly affecting fetus   11599001
  • Hereditary disorder by system   363137000
  • Hereditary dysplasminogenemia   95845002
  • Hereditary folate deficiency anemia   735453008
  • Hereditary hemochromatosis   35400008
  • Hereditary hypertyrosinemia   271847005
  • Hereditary hypoplasminogenemia   95841006
  • Hereditary lymphedema   254199006
  • Hereditary thrombophilia   439698008
  • Hereditary vitamin B12 deficiency anemia   735452003
  • Hereditary xanthinuria   54627004
  • Inborn error of metabolism   86095007
  • Inflammatory hereditary disorder   363181008  removed: 2020-01-31
  • Inherited aminoaciduria   698953004
  • Inherited arthrogryposis   28204005
  • Kabuki make-up syndrome   313426007
  • Malan overgrowth syndrome   763795006
  • Marfanoid syndrome De Silva type   732262003
  • Mehes syndrome   716199000
  • Mendelian disorders   363202005
  • Metabolic hereditary disorder   363205007  removed: 2002-07-31
  • Monogenic autoinflammatory syndrome   724593005
  • Obesity due to melanocortin 4 receptor deficiency   717269008
  • Polygenic hereditary disorder   75970008
  • Postaxial polydactyly type A   715704001
  • Postaxial polydactyly type B   715707008
  • Rare non-syndromic intellectual disability   773772001
  • Severe congenital hypochromic anemia with ringed sideroblasts   725463007
  • Sex-linked hereditary disorder   82852009
  • Syndactyly of fingers type 8   715442006
  • Tetraamelia with multiple malformation syndrome   716249009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009

ancestors
sorted most to least specific
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