ORPHA:726053
Congenital amegakaryocytic thrombocytopenia without known causal genetic defect
Synonyms: CAMT without known causal genetic defect
- Type
- Etiological subtype
- Group
- Subtype of disorder
- Inheritance
- Autosomal dominant, Autosomal recessive
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital amegakaryocytic thrombocytopenia without known causal genetic defect | CAMT without known causal genetic defect |
| fr | Thrombocytopénie amégacaryocytaire congénitale sans défaut génétique causal identifié | CAMT sans défaut génétique causal identifié |
| de | Angeborene amegakaryozytäre Thrombozytopenie ohne bekannten ursächlichen Gendefekt | CAMT ohne bekannten ursächlichen Gendefekt |
| es | Trombocitopenia amegacariocítica congénita sin defecto genético causal identificado | TAC sin defecto genético causal identificado |
| it | Trombocitopenia amegacariocitica congenita senza difetto genetico noto | CAMT senza difetto genetico noto |
| nl | Congenitale amegakaryocytaire trombocytopenie zonder gekend causaal genetisch defect | CAMT zonder gekend causaal genetisch defect |
| pt | Congenital amegakaryocytic thrombocytopenia without known causal genetic defect | |
| pl | Congenital amegakaryocytic thrombocytopenia without known causal genetic defect | = en |
| cs | Congenital amegakaryocytic thrombocytopenia without known causal genetic defect | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:3319Congenital amegakaryocytic thrombocytopenia
rare genetic diseases; rare hematological diseases; rare transplant-related disorders
No children.
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/726053
- This record as JSON: /data/d/726053.json