Glucocorticoid deficiency with achalasia 45414006
SNOMED CT code
| SNOMED code | 45414006 |
|---|---|
| name | Glucocorticoid deficiency with achalasia |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Glucocorticoid deficiency with achalasia (disorder) |
| synonyms |
|
| attributes - group4 | |
| Finding site | Thyroid structure 69748006 |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Cardioesophageal junction structure 25271004 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Finding site | Adrenal cortex structure 68594002 |
| attributes - group1 | |
| Has interpretation | Abnormal 263654008 |
| Interprets | Motility 398598008 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Disorder of adrenal gland 30171000 Disorder of adrenal cortex 129636003 Adrenal cortical hypofunction 386584007 Primary adrenocortical insufficiency 373662000 Adrenocorticotropic hormone resistance syndrome 1156181008 Glucocorticoid deficiency with achalasia 45414006 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Glucocorticoid deficiency with achalasia 45414006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital achalasia of esophagus 700283004 Glucocorticoid deficiency with achalasia 45414006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Glucocorticoid deficiency with achalasia 45414006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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