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 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 sorted most to least specific
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