Childhood hypophosphatasia   30174008

SNOMED CT code


SNOMED code30174008
nameChildhood hypophosphatasia
statusactive
date introduced2002-01-31
fully specified name(s)Childhood hypophosphatasia (disorder)
synonyms
  • Childhood hypophosphatasia
  • Hypophosphatasia, childhood type
  • Juvenile hypophosphatasia
attributes - group2
OccurrenceCongenital   255399007
attributes - group1
OccurrenceChildhood   255398004
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Inborn error of metabolism   86095007
          Hypophosphatasia   190859005
            Childhood hypophosphatasia   30174008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Enzymopathy   78548001
          Childhood hypophosphatasia   30174008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Childhood hypophosphatasia   30174008

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

demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.