ORPHA:567562
Disorder with multisystemic involvement and glomerulopathy
- 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 glomerulopathy | |
| fr | Maladie avec atteinte multisystémique et glomérulopathie | |
| de | Multisystemische Störung mit Glomerulopathie als Hauptmerkmal | |
| es | Trastorno con afectación multisistémico y glomerulopatía | |
| it | Malattia multisistemica con glomerulopatia | |
| nl | Aandoening met multisystemische betrokkenheid en glomerulopathie | |
| pt | Doença com envolvimento multissistémico e glomerulopatia | |
| pl | Zaburzenie z zajęciem wielu układów i glomerulopatią | |
| cs | Porucha s multisystémovým postižením a glomerulopatií | |
| uk | Захворювання з мультисистемним ураженням та гломерулопатією | |
| zh | 多系统受累伴肾小球病变 | |
| tr | Multisistemik tutulum ve glomerülopati ile seyreden bozukluk |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681301 | 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:183586Genetic glomerular disease
rare genetic diseases - ORPHA:93548Glomerular disease
rare renal diseases; rare transplant-related disorders
Children (17):
- ORPHA:163696Action myoclonus-renal failure syndrome
- ORPHA:93114Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
- ORPHA:69063Congenital membranous nephropathy due to fetomaternal anti-neutral endopeptidase alloimmunization
- ORPHA:220Denys-Drash syndrome
- ORPHA:506334Familial steroid-resistant nephrotic syndrome with adrenal insufficiency
- ORPHA:280406Familial steroid-resistant nephrotic syndrome with sensorineural deafness
- ORPHA:347Frasier syndrome
- ORPHA:2065Galloway-Mowat syndrome
- ORPHA:69735Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
- ORPHA:306504Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome
- ORPHA:182050MYH9-related syndromic thrombocytopenia
- ORPHA:2614Nail-patella syndrome
- ORPHA:2613Nail-patella-like renal disease
- ORPHA:300333Nephrotic syndrome-epidermolysis bullosa-sensorineural deafness syndrome
- ORPHA:2670Pierson syndrome
- ORPHA:1830Schimke immuno-osseous dysplasia
- ORPHA:2715Severe oculo-renal-cerebellar 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/567562
- This record as JSON: /data/d/567562.json