SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Developmental disorder  5294002

Congenital malformation  276654001

Congenital malformation syndrome  400038003

Malformation sequence   105989001

SNOMED CT code


SNOMED code105989001
nameMalformation sequence
statusactive
date introduced2002-01-31
fully specified name(s)Malformation sequence (disorder)
synonymsMalformation sequence
attributes - group1
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
parentsCongenital malformation syndrome   400038003
children
  • Allemann's syndrome   70943004
  • Athyrotic hypothyroidism sequence   55838005
  • Caudal regression syndrome   8301004
  • Exstrophy of urinary bladder sequence   61758007
  • Holoprosencephaly sequence   30915001
  • Immotile cilia syndrome   86204009
  • Jugular lymphatic obstruction sequence   74650009
  • Klippel-Feil sequence   5601008
  • Laterality sequence   24614000
  • Occult spinal dysraphism sequence   70534000
  • Rokitansky sequence   8793008
  • Sirenomelus sequence   91089008  removed: 2017-07-31
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Malformation sequence   105989001

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

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