ORPHA:314709
Primary localized amyloidosis
Synonyms: Localized AL amyloidosis
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Status
- active
This disease is described under AL amyloidosis
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Primary localized amyloidosis | Localized AL amyloidosis |
| fr | Amylose primitive localisée | Amylose AL localisée |
| de | Amyloidose, lokalisierte primäre | AL-Amyloidose, lokalisierte · Immunoglobulinamyloidose, lokalisierte |
| es | Amiloidosis localizada primaria | Amiloidosis de cadena ligera localizada · Amiloidosis inmunoglobulínica localizada |
| it | Amiloidosi localizzata primitiva | Amiloidosi AL localizzata · Amiloidosi immunoglobulinica localizzata |
| nl | Primaire gelokaliseerde amyloïdose | Gelokaliseerde AL amyloïdose · Gelokaliseerde amyloïdose van de immunoglobulinen |
| pt | Amiloidose localizada primária | Amiloidose AL localizada · Amiloidose imunoglobulinica localizada |
| pl | Pierwotna amyloidoza zlokalizowana | Zlokalizowana amyloidoza AL. · Zlokalizowana amyloidoza immunoglobulinowa |
| cs | Primární lokalizovaná amyloidóza | Lokalizovaná AL amyloidóza |
| uk | Первинний локалізований амілоїдоз | Локалізований амілоїдоз AL |
| zh | 原发性局灶性淀粉样变 | 局灶性AL淀粉样变 |
| tr | Primer lokalize amiloidoz | Lokalize AL amiloidoz |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | E85.4 | E | specific | validated |
| ICD-11 | 5D00.0 | NTBT | index | validated |
| MONDO | 0017817 | E | validated | |
| UMLS | C5679901 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:85443AL amyloidosis
rare cardiac diseases; rare neurological diseases; rare renal diseases; rare hematological diseases; rare systemic and rheumatological diseases; rare neoplastic diseases; rare transplant-related disorders
No children.
Codes that Orphanet moved or referred to this one:
- ORPHA:102069OBSOLETE: Hepatic amyloidosis with intrahepatic cholestasis referred to · inactive
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/314709
- This record as JSON: /data/d/314709.json