ORPHA:79214
Disorder of biogenic amine metabolism and transport
- 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 biogenic amine metabolism and transport | |
| fr | Trouble du métabolisme et du transport des amines biogènes | |
| de | Störung des Biogene Amine-Stoffwechsels/-Transports | |
| es | Enfermedad del metabolismo y transporte de aminas biogénicas | |
| it | Difetto del metabolismo e del trasporto delle ammine biogeniche | |
| nl | Stoornis van biogeen aminemetabolisme en -transport | |
| pt | Metabólica da neurotransmissão, anomalia | |
| pl | Zaburzenie metabolizmu i transportu amin biogennych | |
| cs | Poruchy metabolismu a transportu biogenních aminů | |
| uk | Порушення метаболізму та транспорту біогенних амінів | |
| zh | 生物胺代谢和转运异常 | |
| tr | Biyojenik amin metabolizması ve taşınmasında bozukluk |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019250 | E | validated | |
| MONDO | 19250 | E | validated | |
| UMLS | C5681274 | 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:68367Rare inborn error of metabolism
rare inborn errors of metabolism; rare genetic diseases
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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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/79214
- This record as JSON: /data/d/79214.json