Neutropenia, monocytopenia, deafness syndrome   725137007

SNOMED CT code


SNOMED code725137007
nameNeutropenia, monocytopenia, deafness syndrome
statusactive
date introduced2017-07-31
fully specified name(s)Neutropenia, monocytopenia, deafness syndrome (disorder)
synonymsNeutropenia, monocytopenia, deafness syndrome
attributes - group2
Finding siteInner ear structure   22945000
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
attributes - group3
Pathological processAbnormal immune process   769247005
attributes - group4
InterpretsHearing   47078008
attributes - group1
Has interpretationBelow reference range   281300000
InterpretsNeutrophil count   30630007
parents
  • Congenital anomaly of ear with impairment of hearing   111339003
  • Hearing loss associated with syndrome   232333009
  • Congenital anomaly of inner ear   43353004
  • Congenital neutropenia   89655007
  • Congenital deafness   95828007
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital hearing disorder   95827002
          Congenital anomaly of ear with impairment of hearing   111339003
            Neutropenia, monocytopenia, deafness syndrome   725137007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Functional finding   118228005
      Hearing finding   118230007
        Hearing disorder   128540005
          Hearing loss   15188001
            Hearing loss associated with syndrome   232333009
              Neutropenia, monocytopenia, deafness syndrome   725137007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of sensory organ   1279550006
        Disorder of ear   25906001
          Disorder of inner ear   232297009
            Congenital anomaly of inner ear   43353004
              Neutropenia, monocytopenia, deafness syndrome   725137007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital immunodeficiency disease   36138009
          Congenital neutropenia   89655007
            Neutropenia, monocytopenia, deafness syndrome   725137007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital hearing disorder   95827002
          Congenital deafness   95828007
            Neutropenia, monocytopenia, deafness syndrome   725137007

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