ORPHA:686465
Fibrotic hypersensitivity pneumonitis
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Fibrotic hypersensitivity pneumonitis | |
| fr | Pneumopathie d'hypersensibilité fibreuse | |
| de | Hypersensitivitätspneumonitis, fibrotische | |
| es | Neumonitis por hipersensibilidad fibrótica | |
| it | Polmonite da ipersensibilità fibrotica | |
| nl | Fibrotische overgevoeligheidspneumonitis | |
| pt | Pneumonite de hipersensibilidade fibrótica | |
| pl | Fibrotic hypersensitivity pneumonitis | |
| cs | Fibrotická hypersenzitivní pneumonitida |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:31740Hypersensitivity pneumonitis
rare respiratory diseases; rare allergic disease; rare transplant-related disorders
No children.
4
Genes
1 direct| Gene | Association | Status | HGNC | Ensembl | OMIM | Locus | Name | Source of validation |
|---|---|---|---|---|---|---|---|---|
| MUC5B | Major susceptibility factor in | Assessed | HGNC:7516 | ENSG00000117983 | 600770 | 11p15.5 | mucin 5B, oligomeric mucus/gel-forming | 28648751[PMID] |
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/686465
- This record as JSON: /data/d/686465.json