SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Developmental disorder  5294002

Disorder of bone development  371521007

Congenital anomaly of skeletal bone  8447006

Chondrodysplasia punctata  278715001

X-linked dominant chondrodysplasia punctata of Happle   403778001

SNOMED CT code


SNOMED code403778001
nameX-linked dominant chondrodysplasia punctata of Happle
statusremoved
date introduced2003-07-31
fully specified name(s)X-linked dominant chondrodysplasia punctata of Happle (disorder)
synonyms
  • X-linked dominant chondrodysplasia punctata of Happle
  • X-linked dominant ichthyosis (Happle)
parentsChondrodysplasia punctata   278715001
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Disorder of bone development   371521007
          Congenital anomaly of skeletal bone   8447006
            Chondrodysplasia punctata   278715001
              X-linked dominant chondrodysplasia punctata of Happle   403778001  removed: 2021-09-30

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:
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