| familiaire angiolipomatose (aandoening) | | familiaire angiolipomatose | | familiale angiolipomatose
| | Familial angiolipomatosis | | A rare genetic subcutaneous tissue disorder with the presence of benign usually multiple subcutaneous tumors. The tumors are composed of adipose tissue and blood vessels typically manifesting as yellow firm circumscribed 1-4 cm in diameter tumors located in the arms, legs and trunk with deep extension of the lesions between muscles, tendons and joint capsules (without infiltration of these structures) in several members of a single family. Tumors may be tender or mildly painful when palpated and do not regress spontaneously. |
| | Id | 774066000 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| SNOMED CT to Orphanet simple map | 199279 |
| SNOMED CT to ICD-10 extended map | | Target | D17.9 | | Rule | TRUE | | Advice | ALWAYS D17.9 | POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE | | Correlation | SNOMED CT source code to target map code correlation not specified |
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