LMNA-related cardiocutaneous progeria syndrome 773426004
SNOMED CT code
| SNOMED code | 773426004 |
|---|---|
| name | LMNA-related cardiocutaneous progeria syndrome |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Lamin A/C related cardiocutaneous progeria syndrome (disorder) |
| synonyms |
|
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Finding site | Skin structure 39937001 |
| attributes - group1 | |
| Finding site | Cardiovascular structure 113257007 |
| 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 LMNA-related cardiocutaneous progeria syndrome 773426004 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Premature aging syndrome 399959003 Laminopathy with premature aging 1177118004 LMNA-related cardiocutaneous progeria syndrome 773426004 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Cardiovascular system hereditary disorder 363005004 LMNA-related cardiocutaneous progeria syndrome 773426004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Hereditary cancer-predisposing syndrome 699346009 LMNA-related cardiocutaneous progeria syndrome 773426004 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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