ORPHA:79253
Mild phenylketonuria
inactive · moved to ORPHA:716Phenylketonuria
Synonyms: Mild PKU · Variant PKU · Variant phenylketonuria · mPKU
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Phenylketonuria
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Mild phenylketonuria | Mild PKU · Variant PKU · Variant phenylketonuria · mPKU |
| fr | Phénylcétonurie modérée | PCU atypique · PCU modérée · PKU modérée · Phénylcétonurie atypique · Variant PKU · mPCU · mPKU |
| de | Phenylketonurie, milde | PKU, milde · Phenylketonurie, Variante · mPKU |
| es | Fenilcetonuria leve | PKU leve · Variante de la PKU · Variante de la fenilcetonuria · mPKU |
| it | Fenilchetonuria lieve | PKU lieve · Variante della PKU · Variante della fenilchetonuria · mPKU |
| nl | Milde fenylketonurie | Afwijkende PKU · Afwijkende fenylketonurie · Milde PKU · mPKU |
| pt | Fenilcetonúria ligeira | PKU ligeira · Variante da PKU · Variante da fenilcetonúria |
| pl | Fenyloketonuria łagodna | mPKU · PKU łagodna · Wariant fenylketonurii · Wariant PKU |
| cs | Mírná fenylketonurie | Mírná PKU · Variantní PKU · Variantní fenylketonurie · mPKU |
| uk | Легка фенілкетонурія | Легка форма ФКУ · mPKU · Варіантна фенілкетонурії · Варіантна ФКУ |
| zh | 轻型苯丙酮尿症 | 变异型苯丙酮尿症 |
| tr | Hafif fenilketonüri | mPKU · Hafif PKU · Varyant PKU · Varyant fenilketonüri |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019258 | E | validated | |
| UMLS | C5680203 | E | validated | |
| GARD | 10324 | 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
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/79253
- This record as JSON: /data/d/79253.json