ORPHA:568044
Primary lymphedema with systemic or visceral involvement
- 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
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Primary lymphedema with systemic or visceral involvement | |
| fr | Lymphoedème primaire avec atteinte systémique ou viscérale | |
| de | Primäres Lymphödem mit systemischer und viszeraler Beteiligung | |
| es | Linfedema primario con afectación sistémica o visceral | |
| it | Linfedema primitivo sistemico o viscerale | |
| nl | Primair lymfoedeem met systemische of viscerale betrokkenheid | |
| pt | Linfedema primário com envolvimento sistémico ou visceral | |
| pl | Pierwotny obrzęk limfatyczny ze zmianami układowymi lub trzewnymi | |
| cs | Primární lymfedém se systémovým nebo viscerálním postižením | |
| uk | Первинна лімфедема із системним або вісцеральним ураженням | |
| zh | 全身或内脏受累型原发性淋巴水肿 | |
| tr | Sistemik veya viseral tutulum ile seyreden primer lenfödem |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681304 | 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:77240Primary lymphedema
rare developmental anomalies during embryogenesis; rare genetic diseases; rare skin diseases; rare circulatory system diseases
Children (9):
- ORPHA:1116Aplasia cutis congenita-intestinal lymphangiectasia syndrome
- ORPHA:1563Dahlberg-Borer-Newcomer syndrome
- ORPHA:568065EPHB4-related lymphatic-related hydrops fetalis
- ORPHA:2136Hennekam syndrome
- ORPHA:69735Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
- ORPHA:662Lymphedema with yellow nails
- ORPHA:86915Lymphedema-atrial septal defects-facial changes syndrome
- ORPHA:568062PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis
- ORPHA:568056Warts-immunodeficiency-lymphedema-anogenital dysplasia 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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/568044
- This record as JSON: /data/d/568044.json