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
  • Atypical cystic fibrosis   762270003
  • Auditory system hereditary disorder   362991006
  • Autosomal recessive facio-digito-genital syndrome   725434009
  • Bilateral multiple fibroadenoma of breast   716658005
  • BSG syndrome   719097002
  • Cardiovascular system hereditary disorder   363005004
  • Chronic respiratory distress with surfactant metabolism deficiency   783182004
  • Classical cystic fibrosis   762269004
  • Corticosteroid-binding globulin deficiency   773728004
  • Digestive system hereditary disorder   363080007
  • Familial cancer of breast   254843006
  • Familial isolated congenital asplenia   726708009
  • Familial isolated hyperparathyroidism   786037006
  • Familial juvenile hypertrophy of the breast   770436006
  • Familial nonmedullary thyroid carcinoma   786038001
  • Familial spontaneous pneumothorax   715219001
  • Hand-foot-genital syndrome   702425002
  • 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
  • Insulin resistance - type A   237651005
  • Nakajo-Nishimura syndrome   702449004
  • OTULIN-related autoinflammatory syndrome   765435009
  • Pseudohypoparathyroidism type 1C   717792007
  • Pulmonary interstitial glycogenosis   707551007
  • Pulmonary lipid storage disease   233720006
  • Reproductive system hereditary disorder   363290007
  • Splenomegaly co-occurrent and due to storage disease   724638006
  • Subclinical cystic fibrosis   762271004
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
    Finding by site   118234003
      Disorder by body site   123946008
        Disorder of body system   362965005
          Hereditary disorder by system   363137000

ancestors
sorted most to least specific
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