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
  • Chronic granulomatous disease   387759001
  • Connective tissue hereditary disorder   363045008
  • Developmental hereditary disorder   363070008
  • Familial hemorrhagic diathesis   6935003
  • Familial thyroglossal duct cyst   717331000
  • Fetus with hereditary disease   199531009
  • Genetic syndrome   290028006  removed: 2019-07-31
  • Hereditary amyloidosis   367601000119103
  • Hereditary angioedema   82966003
  • 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 hypoplasminogenemia   95841006
  • Hereditary iron deficiency anemia   1153403009
  • Hereditary metabolic disease   1821000146108
  • Hereditary thrombophilia   439698008
  • Hereditary vitamin B12 deficiency anemia   735452003
  • Inflammatory hereditary disorder   363181008  removed: 2020-01-31
  • Maternally inherited mitochondrial deoxyribonucleic acid disease   1162975000
  • Mendelian disorders   363202005
  • Mendelian susceptibility to mycobacterial disease   1172895006
  • Metabolic hereditary disorder   363205007  removed: 2002-07-31
  • Obesity due to melanocortin 4 receptor deficiency   717269008
  • Polygenic hereditary disorder   75970008
  • Sea-blue histiocyte syndrome   37821003
  • Severe congenital hypochromic anemia with ringed sideroblasts   725463007
  • Sex-linked hereditary disorder   82852009
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
cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts.  Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:
  • CPT® to SNOMED Crosswalks

demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.