ORPHA:309340
Disorder of lysosomal-related organelles
- 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 | Disorder of lysosomal-related organelles | |
| fr | Anomalie des organelles type lysosomes | |
| de | Störung der Lysosomen-verwandten Organellen | |
| es | Trastornos de los orgánulos relacionados con los lisosomas | |
| it | Difetto degli organelli associati ai lisosomi | |
| nl | Stoornis van lysosomaal-gerelateerde organellen | |
| pt | Doença de organelas lisossoma-relacionado | |
| pl | Zaburzenia organelli związanych z lizosomami | |
| cs | Poruchy organel blízkých lysozomům | |
| uk | Хвороба лізосом-повязаних органел | |
| zh | 溶酶体相关细胞器紊乱 | |
| tr | Lizozomal-ilişkili organellerin bozukluğu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0017739 | E | validated | |
| MONDO | 17739 | E | validated | |
| UMLS | C5681043 | 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:68367Rare inborn error of metabolism
rare inborn errors of metabolism; 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/309340
- This record as JSON: /data/d/309340.json