ORPHA:69
Amyloidosis
- Type
- Category
- Group
- Group of disorders
- Age of onset
- All ages
- Status
- active
A vast group of rare systemic diseases characterized by the presence of insoluble fibrillar protein deposits in tissues. Amyloidoses are classified according to biochemical type of amyloid protein involved.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Amyloidosis | |
| fr | Amylose | Amyloïdose |
| de | Amyloidose | |
| es | Amiloidosis | |
| it | Amiloidosi | |
| nl | Amyloïdose | |
| pt | Amiloidose | |
| pl | Amyloidoza | |
| cs | Amyloidóza | |
| uk | Амілоїдоз | |
| zh | 淀粉样变性 | |
| tr | Amiloidoz |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | E85.0 | E | specific | validated |
| ICD-11 | 5D00 | E | specific | validated |
| MONDO | 0019065 | E | validated | |
| MONDO | 19065 | E | validated | |
| MeSH | D000686 | E | validated | |
| UMLS | C0002726 | E | validated | |
| MedDRA | 10002022 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:182222Rare systemic disease
rare systemic and rheumatological diseases
Children (12):
- ORPHA:85445AA amyloidosis
- ORPHA:439232AApoAIV amyloidosis
- ORPHA:439246ABeta2M amyloidosis
- ORPHA:85448AGel amyloidosis
- ORPHA:442582AH amyloidosis
- ORPHA:85443AL amyloidosis
- ORPHA:439224ALECT2 amyloidosis
- ORPHA:271861Hereditary ATTR amyloidosis
- ORPHA:85450Hereditary amyloidosis with primary renal involvement
- ORPHA:85458Hereditary cerebral amyloid angiopathy
- ORPHA:439254ITM2B amyloidosis
- ORPHA:330001Wild type ATTR amyloidosis
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
| Point prevalence | 1-9 / 100 000 | 1.91 / 100 000 | Korea, Republic of | Value and class | Validated | 28877709[PMID] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/69
- This record as JSON: /data/d/69.json