Primary hypogonadism   370999003


SNOMED code370999003
namePrimary hypogonadism
date introduced2002-07-31
fully specified name(s)Primary hypogonadism (disorder)
  • Primary hypogonadism
  • Hypergonadotropic hypogonadism
attributes - group1
Finding siteGonadal endocrine structure   304041004
parentsHypogonadism   48130008
  • Alopecia and intellectual disability with hypergonadotropic hypogonadism syndrome   720981000
  • Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome   719451006
  • Hydrocephalus with obesity and hypogonadism syndrome   721231007
  • Hypergonadotropic hypogonadism with cataract syndrome   721233005
  • Hypogonadism with mitral valve prolapse and intellectual disability syndrome   721841001
  • Intellectual disability, craniofacial dysmorphism, hypogonadism, diabetes mellitus syndrome   722454003
  • Microcephalus, hypergonadotropic hypogonadism, short stature syndrome   733092009
  • Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome   724097003
  • Primary hypergonadotropic hypogonadism and partial alopecia syndrome   719275009
  • Primary ovarian failure   65846009
  • Primary testicular failure   370997001
  • Woodhouse Sakati syndrome   816067005
  • X-linked intellectual disability Cilliers type   719013004
  • X-linked intellectual disability Van Esch type   718914002
  • X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome   765471005
a selection of possible paths
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

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