Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome   721842008

SNOMED CT code


SNOMED code721842008
nameHypogonadotropic hypogonadism with frontoparietal alopecia syndrome
statusactive
date introduced2017-01-31
fully specified name(s)Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome (disorder)
synonyms
  • Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome
  • Salti Salem syndrome
attributes - group1
Associated morphologyAbsence   418560003
OccurrenceCongenital   255399007
Finding siteHair structure   386045008
attributes - group2
OccurrenceCongenital   255399007
Finding siteGonadal endocrine structure   304041004
attributes - group4
OccurrenceCongenital   255399007
Finding siteStructure of distal part of pituitary   52618001
parents
  • Autosomal dominant hereditary disorder   11164009
  • Hereditary disorder of endocrine system   363104002
  • Hereditary disorder of the integument   363185004
  • Hereditary disorder of nervous system   363235000
  • Reproductive system hereditary disorder   363290007
  • Alopecia   56317004
  • Congenital hypogonadotropic hypogonadism   722944006
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
              Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome   721842008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Hereditary disorder of endocrine system   363104002
          Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome   721842008

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
            Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome   721842008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Disorder by body site   123946008
        Disorder of body system   362965005
          Disorder of nervous system   118940003
            Hereditary disorder of nervous system   363235000
              Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome   721842008

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
              Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome   721842008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding by site   118234003
      Integumentary system finding   106077005
        Skin finding   106076001
          Hair finding   247522004
            Disorder of hair   279425004
              Alopecia   56317004
                Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome   721842008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital hypogonadotropic hypogonadism   722944006
          Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome   721842008

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.