Membranous congenital glomerulonephritis due to anti-maternal neutral endopeptidase alloimmunization
General Information (adopted from Orphanet):
| Synonyms, Signs: |
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| Number of Symptoms | 1 |
| OrphanetNr: | 69063 |
| OMIM Id: |
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| ICD-10: |
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| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
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Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Autosomal recessive [Orphanet] |
| Age of onset: |
Antenatal Neonatal [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Primary glomerular disease
-Rare genetic disease -Rare renal disease |
Symptom Information:
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(HPO:0000100) | Nephrotic syndrome | Very frequent [Orphanet] | 83 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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