Carney complex 733491005
SNOMED CT code
| SNOMED code | 733491005 |
|---|---|
| name | Carney complex |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Carney complex (disorder) |
| synonyms |
|
| attributes - group3 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Structure of multiple endocrine glands 77637002 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Myxomatous neoplasm 115226005 |
| Finding site | Heart structure 80891009 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Skin structure 39937001 |
| Associated morphology | Hyperpigmentation 4830009 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Carney complex 733491005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Disorder of skin pigmentation 46690002 Congenital pigmentary skin anomalies 205564003 Carney complex 733491005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Polyglandular dysfunction AND/OR related disorders 26572003 Polyglandular dysfunction 111546006 Polyglandular hyperfunction 237827002 Carney complex 733491005 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Cardiovascular system hereditary disorder 363005004 Carney complex 733491005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Carney complex 733491005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Carney complex 733491005 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Carney complex 733491005 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Neoplasm of intrathoracic organs 126638003 Neoplasm of heart 387842002 Myxoma of heart 426191007 Carney complex 733491005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Disorder of skin pigmentation 46690002 Hyperpigmentation of skin 49765009 Carney complex 733491005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Genetic disorder of skin pigmentation 724839001 Carney complex 733491005 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Congenital cardiovascular disorder 762228008 Carney complex 733491005 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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