Hypogonadotropic hypogonadism retinitis pigmentosa syndrome   733113002

SNOMED CT code


SNOMED code733113002
nameHypogonadotropic hypogonadism retinitis pigmentosa syndrome
statusactive
date introduced2017-07-31
fully specified name(s)Hypogonadotropic hypogonadism retinitis pigmentosa syndrome (disorder)
synonyms
  • Hypogonadotropic hypogonadism retinitis pigmentosa syndrome
  • Chang Davidson Carlson syndrome
attributes - group3
Associated morphologyDystrophy   4720007
OccurrenceCongenital   255399007
Finding siteRetinal structure   5665001
attributes - group4
OccurrenceCongenital   255399007
Finding siteGonadal endocrine structure   304041004
attributes - group5
OccurrenceCongenital   255399007
Finding siteStructure of distal part of pituitary   52618001
parents
  • Retinitis pigmentosa   28835009
  • Hereditary disorder of endocrine system   363104002
  • Hereditary disorder of nervous system   363235000
  • Reproductive system hereditary disorder   363290007
  • Congenital hypogonadotropic hypogonadism   722944006
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Visual system disorder   128127008
        Hereditary disorder of the visual system   363343008
          Hereditary retinal dystrophy   41799005
            Retinitis pigmentosa   28835009
              Hypogonadotropic hypogonadism retinitis pigmentosa syndrome   733113002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of endocrine system   362969004
          Hereditary disorder of endocrine system   363104002
            Hypogonadotropic hypogonadism retinitis pigmentosa syndrome   733113002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of nervous system   118940003
          Hereditary disorder of nervous system   363235000
            Hypogonadotropic hypogonadism retinitis pigmentosa syndrome   733113002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Hereditary disorder by system   363137000
          Reproductive system hereditary disorder   363290007
            Hypogonadotropic hypogonadism retinitis pigmentosa syndrome   733113002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital hypogonadotropic hypogonadism   722944006
          Hypogonadotropic hypogonadism retinitis pigmentosa syndrome   733113002

ancestors
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