ORPHA:415286
Bilirubin encephalopathy
Synonyms: Kernicterus
- Type
- Clinical group
- Group
- Group of disorders
- Inheritance
- Not applicable
- Age of onset
- Infancy, Neonatal
- 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 | Bilirubin encephalopathy | Kernicterus |
| fr | Encéphalopathie bilirubinique | Ictère nucléaire |
| de | Bilirubin-Enzephalopathie | Kernikterus |
| es | Encefalopatía bilirrubínica | Kernícterus |
| it | Encefalopatia da bilirubina | Kernittero |
| nl | Bilirubine-encefalopathie | = en |
| pt | Encefalopatia bilirrubinica | |
| pl | Encefalopatia bilirubinowa | Żółtaczka jąder podkorowych mózgu |
| cs | Bilirubinová encefalopatie | Kernikterus |
| uk | Білірубінова енцефалопатія | = en |
| zh | 胆红素脑病 | 胆红素脑病 |
| tr | Bilirubin ensefalopatisi | Kernikterus |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | P57 | E | specific | validated |
| MONDO | 0018477 | E | validated | |
| MONDO | 18477 | E | validated | |
| MeSH | D007647 | E | validated | |
| UMLS | C0022610 | E | validated | |
| GARD | 6830 | E | validated | |
| MedDRA | 10023376 | 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 (2):
- ORPHA:309816Disorder of bilirubin metabolism and excretion
rare inborn errors of metabolism - ORPHA:68385Neurometabolic disease
rare neurological diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | 15254556[PMID] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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/415286
- This record as JSON: /data/d/415286.json