Dr Z's Coding References
Cardiothoracic Surgery
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Hereditary disorder by system 363137000 SNOMED CT code SNOMED code 363137000 name Hereditary disorder by system status active date introduced 2002-01-31 fully specified name(s) Hereditary disorder by system (disorder) synonyms Hereditary disorder by system attributes - group1 Finding site Body 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 404684003 64572001 782964007 32895009 363137000 138875005 404684003 118234003 123946008 362965005 363137000 ancestors sorted most to least specific
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