Leydig cell agenesis   56212008

SNOMED CT code


SNOMED code56212008
nameLeydig cell agenesis
statusactive
date introduced2002-01-31
fully specified name(s)Leydig cell agenesis (disorder)
synonyms
  • Leydig cell hypoplasia
  • Leydig cell agenesis
  • Gonadotropin unresponsiveness syndrome
  • Leydig cell dysgenesis
  • Gonadotrophin unresponsiveness syndrome
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyHypoplasia   55199003
Finding siteStructure of interstitial cell of Leydig   44185004
OccurrenceCongenital   255399007
parents
  • Congenital connective tissue disorder   363039000
  • Connective tissue hereditary disorder   363045008
  • Developmental hereditary disorder   363070008
  • Hereditary disorder of endocrine system   363104002
  • Reproductive system hereditary disorder   363290007
  • Congenital anomaly of endocrine testis   371122009
  • Congenital hypoplasia of testis   85437001
  • Autosomal recessive hereditary disorder   85995004
children
  • Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation   1003437009
  • Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation   1003438004
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of connective tissue   105969002
        Congenital connective tissue disorder   363039000
          Leydig cell agenesis   56212008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of connective tissue   105969002
        Connective tissue hereditary disorder   363045008
          Leydig cell agenesis   56212008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Leydig cell agenesis   56212008

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
            Leydig cell agenesis   56212008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Hereditary disorder by system   363137000
          Reproductive system hereditary disorder   363290007
            Leydig cell agenesis   56212008

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
              Congenital anomaly of endocrine testis   371122009
                Leydig cell agenesis   56212008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of trunk structure   302292003
      Finding of abdominopelvic segment of trunk   822987005
        Urogenital finding   118238000
          Genital finding   300479008
            Congenital malformation of genital organs   204821009
              Congenital anomaly of male genital system   4406004
                Congenital hypoplasia of testis and scrotum   15965901000119108
                  Congenital hypoplasia of testis   85437001
                    Leydig cell agenesis   56212008

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Leydig cell agenesis   56212008

ancestors
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