ORPHA:444116
Hereditary amyloidosis
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hereditary amyloidosis | |
| fr | Amylose héréditaire | Amyloïdose héréditaire |
| de | Amyloidose, hereditäre | |
| es | Amiloidosis hereditaria | |
| it | Amiloidosi ereditaria | |
| nl | Hereditaire amyloïdose | Erfelijke amyloïdose |
| pt | Amiloidose hereditária | |
| pl | Amyloidoza dziedziczna | |
| cs | Hereditání amyloidóza | |
| uk | Спадковий амілоїдоз | |
| zh | 遗传性淀粉样变性 | |
| tr | Kalıtsal amiloidoz |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 5D00.2 | E | specific | validated |
| MONDO | 0018634 | E | validated | |
| MONDO | 18634 | E | validated | |
| MeSH | D028226 | E | validated | |
| UMLS | C0740340 | E | validated | |
| GARD | 6611 | E | validated | |
| MedDRA | 10016202 | 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:271870Rare genetic systemic or rheumatologic disease
rare genetic diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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/444116
- This record as JSON: /data/d/444116.json