Diffuse mesangial sclerosis
Symptom Information:
Symptom ID: | HPO:0001967 | |||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the genitourinary system(HPO:0000119) Abnormality of the urinary system(HPO:0000079) Abnormality of the upper urinary tract(HPO:0010935) Abnormality of the kidney(HPO:0000077) Abnormal renal morphology(HPO:0012210) Abnormality of the nephron(HPO:0012575) Abnormality of the glomerulus(HPO:0000095) Mesangial abnormality(HPO:0001966) Diffuse mesangial sclerosis(HPO:0001967) MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Nephropathies and tubular disorders NEC(MedDRA:10029150) Diffuse mesangial sclerosis(HPO:0001967) |
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Database Frequency: | 11 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Congenital nephrotic syndrome, Finnish type | (Orphanet:839) |
Denys-Drash syndrome | (Orphanet:220) |
Familial idiopathic steroid-resistant nephrotic syndrome | (Orphanet:656) |
Familial steroid-resistant nephrotic syndrome with sensorineural deafness | (Orphanet:280406) |
Galloway-Mowat syndrome | (Orphanet:2065) |
MESANGIAL SCLEROSIS, DIFFUSE RENAL, WITH OCULAR ABNORMALITIES | (OMIM:249660) |
NEPHROTIC SYNDROME, TYPE 3 | (OMIM:610725) |
NEPHROTIC SYNDROME, TYPE 4 | (OMIM:256370) |
NEPHROTIC SYNDROME, TYPE 8 | (OMIM:615244) |
Pierson syndrome | (Orphanet:2670) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |