ORPHA:664450
Inherited cancer-predisposing lymphoproliferative syndrome
- 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.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Inherited cancer-predisposing lymphoproliferative syndrome | |
| fr | Syndrome lymphoprolifératif héréditaire prédisposant aux cancers | |
| de | Hereditäres Lymphoproliferatives Syndrom mit Krebsprädisposition | |
| es | Síndrome linfoproliferativo hereditario con predisposición al cáncer | |
| it | Sindrome ereditaria linfoproliferativa predisponente ai tumori | |
| nl | Erfelijk lymfoproliferatief syndroom met tumorpredispositie | |
| pt | Síndrome de cancro hereditário-predisposição linfoproliferativa | |
| pl | Dziedziczny zespół limfoproliferacyjny predysponujący do nowotworów | |
| cs | Dědičný lymfoproliferativní syndrom predisponující k nádorovým onemocněním | |
| uk | Спадковий лімфопроліферативний синдром, що призводить до раку |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5925057 | 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 (1):
- ORPHA:140162Inherited cancer-predisposing syndrome
rare genetic diseases; rare neoplastic diseases
Children (25):
- ORPHA:3261Autoimmune lymphoproliferative syndrome
- ORPHA:436159Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency
- ORPHA:3453Autoimmune polyendocrinopathy type 1
- ORPHA:238505Combined immunodeficiency due to CD27 deficiency
- ORPHA:697389Combined immunodeficiency due to HELIOS deficiency
- ORPHA:538963Combined immunodeficiency due to ITK deficiency
- ORPHA:695172Combined immunodeficiency due to dimerization defective IKAROS mutation
- ORPHA:275523Dianzani autoimmune lymphoproliferative disease
- ORPHA:542301EBV-induced lymphoproliferative disease due to CARMIL2 deficiency
- ORPHA:664726EBV-induced lymphoproliferative disease due to CD137 deficiency
- ORPHA:538958EBV-induced lymphoproliferative disease due to CD70 deficiency
- ORPHA:420573EBV-induced lymphoproliferative disease due to CTPS1 deficiency
- ORPHA:664711EBV-induced lymphoproliferative disease due to PRKCD deficiency
- ORPHA:664699EBV-induced lymphoproliferative disease due to RASGRP1 deficiency
- ORPHA:664729EBV-induced lymphoproliferative disease due to TET2 deficiency
- ORPHA:619948Early-onset autoimmunity-autoinflammation-immunodeficiency syndrome due to SOCS1 haploinsufficiency
- ORPHA:306550FADD-related immunodeficiency
- ORPHA:540Familial hemophagocytic lymphohistiocytosis
- ORPHA:695807Immunodeficiency-systemic inflammation-lymphoma predisposition syndrome
- ORPHA:696874NFKB1-related immune dysregulation
- ORPHA:268114RAS-associated autoimmune leukoproliferative disease
- ORPHA:391487STAT1-related autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome
- ORPHA:438159STAT3-related early-onset multisystem autoimmune disease
- ORPHA:538931X-linked lymphoproliferative disease due to SAP deficiency
- ORPHA:317476XMEN
Codes that Orphanet moved or referred to this one:
- ORPHA:238510OBSOLETE: Lymphoproliferative syndrome referred to · inactive
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/664450
- This record as JSON: /data/d/664450.json