Isolated congenital adermatoglyphia   763748007

SNOMED CT code


SNOMED code763748007
nameIsolated congenital adermatoglyphia
statusactive
date introduced2018-07-31
fully specified name(s)Isolated congenital adermatoglyphia (disorder)
synonyms
  • Isolated congenital adermatoglyphia
  • Congenital absence of fingerprints
  • Immigration delay disease
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyAbsence   418560003
OccurrenceCongenital   255399007
Finding siteEntire dermatoglyphic patterns   314292007
parents
  • Autosomal dominant hereditary disorder   11164009
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of the integument   363185004
  • Abnormal dermatoglyphic pattern   83145004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Isolated congenital adermatoglyphia   763748007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Isolated congenital adermatoglyphia   763748007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Hereditary disorder of the integument   363185004
          Isolated congenital adermatoglyphia   763748007

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Integumentary system finding   106077005
      Disorder of integument   128598002
        Congenital anomaly of integument   38164009
          Congenital anomaly of skin   199879009
            Abnormal dermatoglyphic pattern   83145004
              Isolated congenital adermatoglyphia   763748007

ancestors
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