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SNOMED CT code SNOMED code 190905008 name Cystic fibrosis status active date introduced 2002-01-31 fully specified name(s) Cystic fibrosis (disorder) synonyms Cystic fibrosis CF - Cystic fibrosis Fibrocystic disease Mucoviscidosis attributes - group1 Has interpretation Impaired 260379002 Interprets Mucociliary clearance 63533009 attributes - group2 Finding site Respiratory tract structure 321667001 parents Inherited mucociliary clearance defect 233661002 Autosomal recessive hereditary disorder 85995004 children Atypical cystic fibrosis 762270003 Classical cystic fibrosis 762269004 Cystic fibrosis due to heterozygous deltaF508 mutation 1296527009 Cystic fibrosis due to homozygous deltaF508 mutation 1296528004 Cystic fibrosis NOS 190911006 removed: 2010-01-31 Cystic fibrosis of pancreas 235978006 Cystic fibrosis of the lung 86555001 Cystic fibrosis with gastritis and megaloblastic anemia syndrome 720401009 Cystic fibrosis with intestinal manifestations 190909002 removed: 2020-01-31 Cystic fibrosis with meconium ileus 86092005 Cystic fibrosis with no meconium ileus 190906009 removed: 2002-07-31 Cystic fibrosis with other manifestations 307732006 removed: 2010-01-31 Cystic fibrosis with pulmonary manifestations 190908005 removed: 2002-07-31 Cystic fibrosis without meconium ileus 81423003 Diabetes mellitus associated with cystic fibrosis 426705001 Fetal cystic fibrosis 725052002 Follicular hamartoma with alopecia and cystic fibrosis syndrome 716088000 Subclinical cystic fibrosis 762271004 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 118228005 233660001 233661002 190905008 138875005 404684003 64572001 782964007 32895009 1899006 85995004 190905008 ancestors sorted most to least specific
cpt crosswalks Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.
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