ORPHA:568047
Disorder with multisystemic involvement and primary lymphedema
- 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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Disorder with multisystemic involvement and primary lymphedema | |
| fr | Maladie avec atteinte multisystémique et lymphoedème primaire | |
| de | Störung mit multisystemischer Beteiligung und primären Lymphödem | |
| es | Trastorno con afectación multisistémica y linfedema primario | |
| it | Malattia multisistemica e linfedema primitivo | |
| nl | Aandoening met multisystemische betrokkenheid en primair lymfoedeem | |
| pt | Doença com envolvimento multissistémico e linfedema primário | |
| pl | Zaburzenie z zajęciem wielu układów i pierwotnym obrzękiem limfatycznym | |
| cs | Porucha s multisystémovým postižením a primárním lymfedémem | |
| uk | Захворювання з мультисистемним ураженням та первинною лімфедемою | |
| zh | 原发性淋巴水肿伴多系统受累 | |
| tr | Multisistemik tutulum ve primer lenfödem ile seyreden bozukluk |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681303 | 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 (1):
- ORPHA:77240Primary lymphedema
rare developmental anomalies during embryogenesis; rare genetic diseases; rare skin diseases; rare circulatory system diseases
Children (13):
- ORPHA:1340Cardiofaciocutaneous syndrome
- ORPHA:324Fabry disease
- ORPHA:69088Hypohidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome
- ORPHA:1655Müllerian derivatives-lymphangiectasia-polydactyly syndrome
- ORPHA:648Noonan syndrome
- ORPHA:2710Oculodentodigital dysplasia
- ORPHA:2836PEHO syndrome
- ORPHA:99807PEHO-like syndrome
- ORPHA:48652Phelan-McDermid syndrome
- ORPHA:742Prolidase deficiency
- ORPHA:487796Takenouchi-Kosaki syndrome
- ORPHA:805Tuberous sclerosis complex
- ORPHA:881Turner syndrome
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/568047
- This record as JSON: /data/d/568047.json