Hereditary disorder by system   363137000

SNOMED CT code


SNOMED code363137000
nameHereditary disorder by system
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary disorder by system (disorder)
synonymsHereditary disorder by system
attributes - group1
Finding siteBody system structure   91689009
parents
children
  • AHDC1-related intellectual disability, obstructive sleep apnea, mild dysmorphism syndrome   774068004
  • Albinism co-occurrent with hematologic disorder   366961000119106
  • Auditory system hereditary disorder   362991006
  • Autosomal recessive facio-digito-genital syndrome   725434009
  • Cardiovascular system hereditary disorder   363005004
  • Chronic respiratory distress with surfactant metabolism deficiency   783182004
  • Digestive system hereditary disorder   363080007
  • Emberger syndrome   700057001
  • Familial cancer of breast   254843006
  • Familial isolated congenital asplenia   726708009
  • Familial juvenile hypertrophy of the breast   770436006
  • Familial spontaneous pneumothorax   715219001
  • Hand-foot-genital syndrome   702425002
  • Heme oxygenase-1 deficiency   1230003009
  • Hereditary disorder of cellular element of blood   414393003
  • Hereditary disorder of endocrine system   363104002
  • Hereditary disorder of hematologic system   363136009  removed: 2005-01-31
  • Hereditary disorder of immune system   363138005
  • Hereditary disorder of lymphatic system   363190001
  • Hereditary disorder of musculoskeletal system   363212003
  • Hereditary disorder of nervous system   363235000
  • Hereditary disorder of the integument   363185004
  • Hereditary disorder of the urinary system   363338001
  • Hereditary disorder of the visual system   363343008
  • Inherited acute myeloid leukemia   764940002
  • Inherited mucociliary clearance defect   233661002
  • Interstitial lung disease due to ABCA3 deficiency   1222678003
  • Interstitial lung disease due to surfactant protein C deficiency   1222677008
  • Pulmonary interstitial glycogenosis   707551007
  • Reproductive system hereditary disorder   363290007
  • Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency   1228876007
  • Splenomegaly co-occurrent and due to storage disease   724638006  removed: 2021-09-30
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Hereditary disorder by system   363137000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Hereditary disorder by system   363137000

ancestors
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