Focal segmental glomerulosclerosis
Symptom Information:
Symptom ID: | HPO:0000097 | |||||||||||
Synonyms: |
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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) Glomerulosclerosis(HPO:0000096) Focal segmental glomerulosclerosis(HPO:0000097) MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Glomerulonephritis and nephrotic syndrome(MedDRA:10018365) Focal segmental glomerulosclerosis(HPO:0000097) |
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Database Frequency: | 37 / 7739 | |||||||||||
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All diseases associated with this symptom:
Action myoclonus - renal failure syndrome | (Orphanet:163696) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E | (Orphanet:93114) |
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome | (Orphanet:306504) |
Denys-Drash syndrome | (Orphanet:220) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1 | (OMIM:603278) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2 | (OMIM:603965) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO | (OMIM:607832) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO | (OMIM:612551) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 5 | (OMIM:613237) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6 | (OMIM:614131) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7 | (OMIM:616002) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8 | (OMIM:616032) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 9 | (OMIM:616220) |
Familial idiopathic steroid-resistant nephrotic syndrome | (Orphanet:656) |
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation | (Orphanet:93214) |
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes | (Orphanet:93216) |
Familial steroid-resistant nephrotic syndrome with sensorineural deafness | (Orphanet:280406) |
Frasier syndrome | (Orphanet:347) |
GLYCOGEN STORAGE DISEASE Ic | (OMIM:232240) |
Galloway-Mowat syndrome | (Orphanet:2065) |
Glycogen storage disease due to glucose-6-phosphatase deficiency | (Orphanet:364) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | (Orphanet:324525) |
Hyperuricemia - anemia - renal failure | (Orphanet:217330) |
MELAS | (Orphanet:550) |
NEPHROTIC SYNDROME, TYPE 2 | (OMIM:600995) |
NEPHROTIC SYNDROME, TYPE 3 | (OMIM:610725) |
NEPHROTIC SYNDROME, TYPE 4 | (OMIM:256370) |
NEPHROTIC SYNDROME, TYPE 9 | (OMIM:615573) |
PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS | (OMIM:308990) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Proximal renal tubular acidosis | (Orphanet:47159) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Spastic paraplegia - nephritis - deafness | (Orphanet:2820) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |