ORPHA:275523
Dianzani autoimmune lymphoproliferative disease
Synonyms: DALD
- Type
- Disease
- Group
- Disorder
- Inheritance
- Unknown
- Age of onset
- All ages
- Status
- active
Dianzani autoimmune lymphoproliferative disease (DALD) is a very rare disorder characterized by autoimmunity, lymphadenopathy and/or splenomegaly.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Dianzani autoimmune lymphoproliferative disease | DALD |
| fr | Maladie lymphoproliférative auto-immune de Dianzani | = en |
| de | Autoimmun-lymphoproliferative Krankheit vom Typ Dianzani | = en |
| es | Enfermedad linfoproliferativa autoinmune de Dianzani | = en |
| it | Malattia linfoproliferativa autoimmune di Dianzani | = en |
| nl | Auto-immune lymfoproliferatieve ziekte van Dianzani | = en |
| pt | Doença linfoproliferativa autoimune de Dianzani | |
| pl | Autoimmunologiczna choroba limfoproliferacyjna Dianzaniego | = en |
| cs | Dianzaniho autoimunitní lymfoproliferativní nemoc | = en |
| uk | Аутоімунна лімфопроліферативна хвороба Діанцані | = en |
| zh | Dianzani自身免疫性淋巴细胞增生性疾病 | = en |
| tr | Dianzani otoimmün lenfoproliferatif hastalık | = en |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 605233 | E | validated | |
| ICD-10 | D47.9 | NTBT | attributed | validated |
| MONDO | 0011524 | E | validated | |
| MeSH | C535950 | E | validated | |
| UMLS | C2931071 | E | validated | |
| GARD | 9797 | 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
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:169355Immunodeficiency syndrome with autoimmunity
rare genetic diseases; rare immunological diseases; rare transplant-related disorders - ORPHA:664450Inherited cancer-predisposing lymphoproliferative syndrome
rare genetic diseases; rare neoplastic diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET |
| Cases/families | 30 cases | Worldwide | Case(s) | Validated | [EXPERT] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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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/275523
- This record as JSON: /data/d/275523.json