Ghosal hematodiaphyseal dysplasia   389214003

SNOMED CT code


SNOMED code389214003
nameGhosal hematodiaphyseal dysplasia
statusactive
date introduced2003-01-31
fully specified name(s)Ghosal hematodiaphyseal dysplasia (disorder)
synonyms
  • Diaphyseal dysplasia with anaemia
  • Diaphyseal dysplasia with anemia
  • Ghosal hematodiaphyseal dysplasia
  • Ghosal haematodiaphyseal dysplasia
  • Diaphyseal dysplasia anaemia syndrome
  • Diaphyseal dysplasia anemia syndrome
  • Ghosal syndrome
attributes - group2
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Associated morphologyDysplasia   25723000
Finding siteDiaphysis structure   53394001
attributes - group4
InterpretsBone density scan   312681000
Has interpretationAbove reference range   281302008
attributes - group1
Has interpretationBelow reference range   281300000
InterpretsMeasurement of total hemoglobin concentration   441689006
attributes - group3
Has interpretationBelow reference range   281300000
InterpretsRed blood cell count   14089001
parents
  • Dysplasia with increased bone density   254120004
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of musculoskeletal system   363212003
  • Hereditary disorder of cellular element of blood   414393003
  • Congenital anemia   63565007
  • Congenital anomaly of skeletal bone   8447006
  • Autosomal recessive hereditary disorder   85995004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Bone finding   118953000
        Disorder of bone   76069003
          Dysplasia with increased bone density   254120004
            Ghosal hematodiaphyseal dysplasia   389214003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Ghosal hematodiaphyseal dysplasia   389214003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Musculoskeletal finding   106028002
      Disorder of musculoskeletal system   928000
        Hereditary disorder of musculoskeletal system   363212003
          Ghosal hematodiaphyseal dysplasia   389214003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of blood, lymphatics and immune system   299691001
      Disorder of cellular component of blood   414022008
        Hereditary disorder of cellular element of blood   414393003
          Ghosal hematodiaphyseal dysplasia   389214003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital anemia   63565007
          Ghosal hematodiaphyseal dysplasia   389214003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Disorder of bone development   371521007
          Congenital anomaly of skeletal bone   8447006
            Ghosal hematodiaphyseal dysplasia   389214003

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Ghosal hematodiaphyseal dysplasia   389214003

ancestors
sorted most to least specific
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