ORPHA:93593
Nephropathy secondary to a storage or other metabolic disease
- 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 | Nephropathy secondary to a storage or other metabolic disease | |
| fr | Néphropathie secondaire à des maladies de surcharge ou à d'autres maladies métaboliques | |
| de | Nephropathie, sekundäre, durch Speicher- oder Stoffwechselkrankheit | |
| es | Nefropatía secundaria por almacenamiento u otra enfermedad metabólica | |
| it | Nefropatia secondaria a malattia da accumulo o altra malattia metabolica | |
| nl | Nefropathie secundair aan een stapelings- of andere stofwisselingsziekte | |
| pt | Nefropatia secundária a doença de armazenamento ou outra doença metabólica | |
| pl | Nefropatia wtórna do choroby spichrzeniowej lub innej choroby metabolicznej | |
| cs | Nefropatie sekundární z důvodu střádání nebo jiného metabolického onemocnění | |
| uk | Нефропатія, спричинена накопиченням або іншим метаболічним захворюванням | |
| zh | 继发于积贮病或其他代谢疾病的肾病 | |
| tr | Depolamaya veya başka bir metabolik hastalığa sekonder nefropati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681622 | 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 (2):
- ORPHA:98056Rare genetic renal disease
rare genetic diseases - ORPHA:93626Rare renal disease
rare renal diseases
Children (30):
- ORPHA:976Adenine phosphoribosyltransferase deficiency
- ORPHA:60Alpha-1-antitrypsin deficiency
- ORPHA:300547Autosomal recessive infantile hypercalcemia
- ORPHA:371207Congenital disorder of glycosylation with nephropathy as a major feature
- ORPHA:1031Enamel-renal syndrome
- ORPHA:324Fabry disease
- ORPHA:69076Familial renal glucosuria
- ORPHA:2088Fanconi-Bickel syndrome
- ORPHA:352Galactosemia
- ORPHA:620371Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation
- ORPHA:364Glycogen storage disease due to glucose-6-phosphatase deficiency
- ORPHA:2116Hartnup disease
- ORPHA:469Hereditary fructose intolerance
- ORPHA:3467Hereditary xanthinuria
- ORPHA:324525Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation
- ORPHA:206428Hypoxanthine-guanine phosphoribosyltransferase deficiency
- ORPHA:35858Imerslund-Gräsbeck syndrome
- ORPHA:411629Infantile nephropathic cystinosis
- ORPHA:247794Juvenile cataract-microcornea-renal glucosuria syndrome
- ORPHA:411634Juvenile nephropathic cystinosis
- ORPHA:650LCAT deficiency
- ORPHA:3222Phosphoribosylpyrophosphate synthetase superactivity
- ORPHA:738Porphyria
- ORPHA:416Primary hyperoxaluria
- ORPHA:87876Sialidosis type 2
- ORPHA:882Tyrosinemia type 1
- ORPHA:28Vitamin B12-responsive methylmalonic acidemia
- ORPHA:27Vitamin B12-unresponsive methylmalonic acidemia
- ORPHA:905Wilson disease
- ORPHA:912Zellweger 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/93593
- This record as JSON: /data/d/93593.json