Hypogonadism   48130008

SNOMED CT code


SNOMED code48130008
nameHypogonadism
statusactive
date introduced2002-01-31
fully specified name(s)Hypogonadism (disorder)
synonymsHypogonadism
attributes - group1
Finding siteGonadal endocrine structure   304041004
parentsDisorder of endocrine gonad   127345001
children
  • Congenital cataract with deafness and hypogonadism syndrome   722378009
  • Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome   715429006
  • Deafness and hypogonadism syndrome   718714006
  • Female hypogonadism syndrome   16041008
  • Frontonasal dysplasia with alopecia and genital anomaly syndrome   725029001
  • Gonad postablative failure   286918006
  • Hypogonadal obesity   5036006
  • Hypogonadotropic hypogonadism   33927004
  • Male hypogonadism   48723006
  • Microcephalic primordial dwarfism, insulin resistance syndrome   1220596009
  • Primary hypogonadism   370999003
  • Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome   724001005
  • Scholte syndrome   722002002
  • Syndromic X-linked intellectual disability type 7   719160009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of endocrine system   362969004
          Disorder of endocrine gonad   127345001
            Hypogonadism   48130008

ancestors
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