Glomerulonephropathy
Symptom Information:
Symptom ID: | MedDRA:10051920 | ||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Nephropathies and tubular disorders NEC(MedDRA:10029150) Glomerulonephropathy(MedDRA:10051920) |
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Database Frequency: | 4 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Alport syndrome | (Orphanet:88918) |
Autosomal recessive Alport syndrome | (Orphanet:88919) |
LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME | (OMIM:308940) |
X-linked Alport syndrome | (Orphanet:88917) |