Neonatal renal venous thrombosis
Synonyms: NRVT · Neonatal RVT
- Type
- Disease
- Group
- Disorder
- Inheritance
- Unknown
- Age of onset
- Antenatal, Neonatal
- Status
- active
A rare vascular condition characterized by the formation of a thrombus (blood clot) in the renal vein of a newborn infant, typically within the first 28 days of life. This condition can cause renal (kidney) ischemia, and may lead to kidney damage, swelling, and potential loss of kidney function. Neonatal renal vein thrombosis (NRVT) can affect one kidney (unilateral) or both kidneys (bilateral), with the severity of symptoms often depending on the extent of the clot and the number of affected kidneys.
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Neonatal renal venous thrombosis | NRVT · Neonatal RVT |
| fr | Thrombose néonatale des veines rénales | TNVR · Thrombose veineuse rénale néonatale |
| de | Nierenvenenthrombose, neonatale | NRVT |
| es | Trombosis venosa renal neonatal | TVR neonatal |
| it | Trombosi venosa renale neonatale | TVR neonatale · TVRN |
| nl | Neonatale trombose van vena renalis | NRVT · Neonatale RVT · Neonatale renale veneuze trombose |
| pt | Trombose venosa renal neonatal | NRVT · RVT neonatal |
| pl | Zakrzepica żył nerkowych noworodków | = en |
| cs | Novorozenecká trombóza renální žíly | = en |
| uk | Неонатальний тромбоз ниркових вен | Неонатальна RVT · NRVT |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | P29.8 | NTBT | attributed | validated |
| ICD-11 | GB90.3 | NTBT | attributed | validated |
| MONDO | 0971105 | E | validated | |
| MONDO | 971105 | E | validated | |
| UMLS | C5925061 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:93626Rare renal disease
rare renal diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
3 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 1 000 000 | 0.13 / 100 000 | Canada | Value and class | Validated | 35372933[PMID]_ORPHANET |
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET |
| Annual incidence | 1-9 / 1 000 000 | 0.11 / 100 000 | Germany | Value and class | Validated | 10653328[PMID]_ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/664912
- This record as JSON: /data/d/664912.json