Progeroid features, hepatocellular carcinoma predisposition syndrome 1216939003
SNOMED CT code
| SNOMED code | 1216939003 |
|---|---|
| name | Progeroid features, hepatocellular carcinoma predisposition syndrome |
| status | active |
| date introduced | 2022-04-30 |
| fully specified name(s) | Progeroid features, hepatocellular carcinoma predisposition syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| attributes - group2 | |
| Finding site | Skin structure 39937001 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Premature aging syndrome 399959003 Progeroid features, hepatocellular carcinoma predisposition syndrome 1216939003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Hereditary cancer-predisposing syndrome 699346009 Progeroid features, hepatocellular carcinoma predisposition syndrome 1216939003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Progeroid features, hepatocellular carcinoma predisposition syndrome 1216939003 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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