Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation 697900005
SNOMED CT code
SNOMED code | 697900005 |
---|---|
name | Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation |
status | active |
date introduced | 2014-01-31 |
fully specified name(s) | Heritable pulmonary arterial hypertension due to activin A receptor type II-like kinase 1 or endoglin mutation (disorder) |
synonyms |
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attributes - group1 | |
Finding site | Pulmonary artery structure 81040000 |
parents | Heritable pulmonary arterial hypertension 697897003 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Cardiovascular finding 106063007 Blood vessel finding 21829004 Arterial finding 248718009 Pulmonary artery finding 251039005 Pulmonary arterial hypertension 11399002 Heritable pulmonary arterial hypertension 697897003 Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation 697900005 |
ancestors | sorted most to least specific
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cpt crosswalks |
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