Congenital isolated adrenocorticotropic hormone deficiency 1231283007
SNOMED CT code
| SNOMED code | 1231283007 |
|---|---|
| name | Congenital isolated adrenocorticotropic hormone deficiency |
| status | active |
| date introduced | 2022-06-30 |
| fully specified name(s) | Congenital isolated adrenocorticotropic hormone deficiency (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Adrenal structure 23451007 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Structure of distal part of pituitary 52618001 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Congenital isolated adrenocorticotropic hormone deficiency 1231283007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Congenital isolated adrenocorticotropic hormone deficiency 1231283007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital isolated adrenocorticotropic hormone deficiency 1231283007 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Disorder of adrenal gland 30171000 Hypoadrenalism 237785004 ACTH deficiency 237692001 Isolated corticotropin deficiency 80599001 Congenital isolated adrenocorticotropic hormone deficiency 1231283007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Congenital isolated adrenocorticotropic hormone deficiency 1231283007 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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