ORPHA:79190
Disorder of phenylalanin or tyrosine metabolism
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Disorder of phenylalanin or tyrosine metabolism | |
| fr | Trouble du métabolisme de la phénylalanine ou de la tyrosine | |
| de | Phenylalanin/Tyrosin-Stoffwechselstörung | |
| es | Enfermedad del metabolismo de la fenilalanina o tirosina | |
| it | Malattia del metabolismo della fenilalanina o tirosina | |
| nl | Stoornis van fenylalanine- of tyrosinemetabolisme | |
| pt | Doença do metabolismo da fenilalanina ou tirosina | |
| pl | Zaburzenie metabolizmu fenyloalaniny i tyrozyny | |
| cs | Poruchy metabolismu fenyalaninu a tyrosinu | |
| uk | Порушення обміну фенілаланіну або тирозину | |
| zh | 苯丙氨酸或酪氨酸代谢异常 | |
| tr | Fenilalanin veya tirozin metabolizması bozukluğu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019235 | E | validated | |
| MONDO | 19235 | E | validated | |
| UMLS | C5681284 | 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:79062Disorder of amino acid and other organic acid 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/79190
- This record as JSON: /data/d/79190.json