Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome   720981000

SNOMED CT code


SNOMED code720981000
nameAlopecia and intellectual disability with hypergonadotropic hypogonadism syndrome
statusactive
date introduced2017-01-31
fully specified name(s)Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome (disorder)
synonyms
  • Devriendt Vandenberghe Fryns syndrome
  • Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome
attributes - group1
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteGonadal endocrine structure   304041004
attributes - group2
Finding siteHair structure   386045008
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Associated morphologyCongenital absence   24216005
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Mental disorder   74732009
        Developmental mental disorder   129104009
          Intellectual disability   110359009
            Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome   720981000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Integumentary system finding   106077005
        Skin finding   106076001
          Disorder of skin   95320005
            Aplasia of skin   254237003
              Congenital alopecia   2965006
                Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome   720981000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary disorder of endocrine system   363104002
          Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome   720981000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Integumentary system finding   106077005
        Disorder of integument   128598002
          Hereditary disorder of the integument   363185004
            Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome   720981000

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
              Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome   720981000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Disorder by body site   123946008
        Disorder of body system   362965005
          Disorder of endocrine system   362969004
            Disorder of endocrine gonad   127345001
              Hypogonadism   48130008
                Primary hypogonadism   370999003
                  Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome   720981000

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.