ORPHA:714046
Primary choroidal lymphoma
Synonyms: PCL
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Elderly
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Primary choroidal lymphoma | PCL |
| fr | Lymphome choroïdien primitif | |
| de | Primäres chorioidales Lymphom | Aderhautmelanom, primäres · PCL |
| es | Linfoma coroideo primario | LCP |
| it | Linfoma primitivo della coroide | = en |
| nl | Primair lymfoom van choroidea | PCL · Primair lymfoom van vaatvlies |
| pt | Primary choroidal lymphoma | |
| pl | Pierwotny chłoniak naczyniówki | = en |
| cs | Primary choroidal lymphoma | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | 69.3 | NTBT | attributed | validated |
| ICD-11 | 2D05 | NTBT | attributed | validated |
| ICD-11 | XH6JB5 | E | specific | 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:279911Primary organ-specific lymphoma
rare hematological diseases; rare neoplastic diseases; rare transplant-related disorders - ORPHA:716210Rare malignant neoplastic choroidal disorder
rare ophthalmic disorders; rare neoplastic diseases
No children.
4
Genes
1 direct| Gene | Association | Status | HGNC | Ensembl | OMIM | Locus | Name | Source of validation |
|---|---|---|---|---|---|---|---|---|
| MYD88 | Disease-causing somatic mutation(s) in | Assessed | HGNC:7562 | ENSG00000172936 | 602170 | 3p22.2 | MYD88 innate immune signal transduction adaptor | 34667996[PMID] |
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET |
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/714046
- This record as JSON: /data/d/714046.json