Alpha-1-antitrypsin deficiency 30188007
SNOMED CT code
| SNOMED code | 30188007 |
|---|---|
| name | Alpha-1-antitrypsin deficiency |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Alpha-1-antitrypsin deficiency (disorder) |
| synonyms |
|
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Finding site | Lung structure 39607008 |
| attributes - group1 | |
| Finding site | Liver structure 10200004 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Viscus structure finding 406123005 Lung finding 301230006 Disorder of lung 19829001 Alpha-1-antitrypsin deficiency 30188007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic and genetic disorder affecting the liver 235903001 Alpha-1-antitrypsin deficiency 30188007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Disorder of glycoprotein metabolism 238045003 Alpha-1-antitrypsin deficiency 30188007 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Alpha-1-antitrypsin deficiency 30188007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Enzymopathy 78548001 Alpha-1-antitrypsin deficiency 30188007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Alpha-1-antitrypsin deficiency 30188007 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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