Partial androgen insensitivity syndrome   122811000119101

SNOMED CT code


SNOMED code122811000119101
namePartial androgen insensitivity syndrome
statusactive
date introduced2015-01-31
fully specified name(s)Partial androgen insensitivity syndrome (disorder)
synonyms
  • Partial androgen insensitivity syndrome
  • Reifenstein syndrome
  • Familial incomplete male pseudohermaphroditism type 1
  • PAIS - partial androgen insensitivity syndrome
attributes - group2
Associated morphologyMorphologically abnormal structure   49755003
Finding siteExternal genitalia structure   77142006
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
attributes - group1
Associated morphologyMorphologically abnormal structure   49755003
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteGonadal endocrine structure   304041004
parents
  • Male pseudohermaphroditism   111332007
  • Androgen resistance syndrome   12313004
  • X-linked hereditary disease   128430005
  • Hereditary disorder of endocrine system   363104002
  • Reproductive system hereditary disorder   363290007
  • Congenital anomaly of endocrine gonad   371118004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Disorder by body site   123946008
        Disorder of trunk   128121009
          Disorder of abdominopelvic segment of trunk   822988000
            Disorder of pelvic region of trunk   609619005
              Male pseudohermaphroditism   111332007
                Partial androgen insensitivity syndrome   122811000119101

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Metabolic disease   75934005
        Disorder of steroid metabolism   28710006
          Androgen resistance syndrome   12313004
            Partial androgen insensitivity syndrome   122811000119101

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Sex-linked hereditary disorder   82852009
            X-linked hereditary disease   128430005
              Partial androgen insensitivity syndrome   122811000119101

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary disorder of endocrine system   363104002
          Partial androgen insensitivity syndrome   122811000119101

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Hereditary disorder by system   363137000
            Reproductive system hereditary disorder   363290007
              Partial androgen insensitivity syndrome   122811000119101

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital anomaly of endocrine gland   4184009
            Congenital anomaly of endocrine gonad   371118004
              Partial androgen insensitivity syndrome   122811000119101

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.