Hypopigmentation-immunodeficiency disease   37548006

SNOMED CT code


SNOMED code37548006
nameHypopigmentation-immunodeficiency disease
statusactive
date introduced2002-01-31
fully specified name(s)Hypopigmentation-immunodeficiency disease (disorder)
synonyms
  • Griscelli syndrome
  • Chediak-Higashi-like syndrome
  • Griscelli syndrome with immunodeficiency
  • Partial albinism with immunodeficiency
  • Hypopigmentation-immunodeficiency disease
attributes - group3
Associated morphologyDecreased melanin pigmentation   37257004
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
attributes - group2
Pathological processAbnormal immune process   769247005
OccurrenceCongenital   255399007
Finding siteImmune system structure   116003000
parents
  • Immunodeficiency associated with multiple organ system abnormalities   234641000
  • Congenital malformation   276654001
  • Congenital immunodeficiency disease   36138009
  • Disturbance of tyrosine metabolism   37200009
  • Disorder of pigmentation   414032001
children
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of immune structure   414030009
          Immunodeficiency with major anomalies   234631003
            Immunodeficiency associated with multiple organ system abnormalities   234641000
              Hypopigmentation-immunodeficiency disease   37548006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Hypopigmentation-immunodeficiency disease   37548006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital immunodeficiency disease   36138009
          Hypopigmentation-immunodeficiency disease   37548006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of organic acid metabolism   116021002
          Disorder of amino acid metabolism   44779003
            Disorder of amino acid and organic acid metabolism   237911005
              Disturbance of tyrosine metabolism   37200009
                Hypopigmentation-immunodeficiency disease   37548006

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of pigmentation   414032001
        Hypopigmentation-immunodeficiency disease   37548006

ancestors
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