Primary membranoproliferative glomerulonephritis
General Information (adopted from Orphanet):
| Synonyms, Signs: |
MPGN Mesangiocapillary glomerulonephritis |
| Number of Symptoms | 4 |
| OrphanetNr: | 54370 |
| OMIM Id: |
305800
609814 614809 615008 |
| ICD-10: |
|
| UMLs: |
C0017662 |
| MeSH: |
D015432 |
| MedDRA: |
10018370 |
| Snomed: |
80321008 |
Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
|
| Age of onset: |
|
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Primary glomerular disease
-Rare genetic disease -Rare renal disease |
Symptom Information:
|
|
(HPO:0000793) | Membranoproliferative glomerulonephritis | 8 / 7739 | ||||
|
|
(HPO:0001693) | Cardiac shunt | 1 / 7739 | ||||
|
|
(HPO:0001939) | Abnormality of metabolism/homeostasis | 328 / 7739 | ||||
|
|
(HPO:0009125) | Lipodystrophy | 54 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
|---|