ORPHA:251312
Overlapping connective tissue disease
- Type
- Clinical group
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Overlapping connective tissue disease | |
| fr | Maladie de chevauchement du tissu conjonctif | |
| de | Mischkollagenose, überlappende | |
| es | Síndrome de solapamiento del tejido conectivo | |
| it | Malattia da sovrapposizione del tessuto connettivo | |
| nl | Overlappende bindweefselziekte | |
| pt | Doença sobreposta do tecido conjuntivo | |
| pl | Nakładająca się choroba tkanki łącznej | |
| cs | Překryvná nemoc pojivové tkáně | |
| uk | Overlap-повʼязана хвороба сполучної тканини | |
| zh | 重叠结缔组织病 | |
| tr | Örtüşen bağ dokusu hastalığı |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | M35.1 | NTBT | specific | validated |
| MONDO | 0016663 | E | validated | |
| MONDO | 16663 | E | validated | |
| UMLS | C1858556 | 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:280373Rare pediatric systemic disease
rare systemic or rheumatologic diseases of childhood - ORPHA:182228Systemic autoimmune disease
rare systemic and rheumatological diseases
Children (1):
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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.
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/251312
- This record as JSON: /data/d/251312.json