SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Neoplasm and/or hamartoma  399981008

Hamartoma  400006008

Congenital hamartoma   399960008

SNOMED CT code


SNOMED code399960008
nameCongenital hamartoma
statusactive
date introduced2003-07-31
fully specified name(s)Congenital hamartoma (disorder)
synonyms
  • Congenital hamartoma
  • Congenital hamartosis
  • Hamartomatous disease
  • Hamartomatosis
attributes - group1
OccurrenceCongenital   255399007
Associated morphologyHamartoma   51398009
parents
children
  • Bilateral congenital hamartoma of irises   16064571000119103
  • Congenital hamartoma of skin   400083002
  • Congenital rhabdomyomatous mesenchymal hamartoma   787472005
  • Cystic hamartoma of lung and kidney   707530009
  • Fibrous skin tumor of tuberous sclerosis   36025004
  • Gardner syndrome   60876000
  • Goltz syndrome   2298005  removed: 2020-01-31
  • Lhermitte-Duclos disease   67944007
  • Neurocutaneous melanosis sequence   208008  removed: 2021-07-31
  • Perlman syndrome   722231005
  • Peutz-Jeghers syndrome   54411001
  • Pulmonary tuberous sclerosis   233718008
  • Riley-Smith syndrome   21984008  removed: 2020-07-31
  • Ruvalcaba-Myhre syndrome   46011003  removed: 2020-07-31
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Neoplasm and/or hamartoma   399981008
        Hamartoma   400006008
          Congenital hamartoma   399960008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital hamartoma   399960008

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.

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