Glomerulosclerosis
Symptom Information:
Symptom ID: | HPO:0000096 | ||||
Synonyms: |
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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) Glomerulosclerosis(HPO:0000096) MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Nephropathies and tubular disorders NEC(MedDRA:10029150) Glomerulosclerosis(HPO:0000096) |
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Database Frequency: | 11 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia | (Orphanet:34149) |
COCKAYNE SYNDROME, TYPE III | (OMIM:216411) |
COENZYME Q10 DEFICIENCY, PRIMARY, 1 | (OMIM:607426) |
Dent disease type 1 | (Orphanet:93622) |
Fabry disease | (Orphanet:324) |
Familial dysautonomia | (Orphanet:1764) |
MEDULLARY CYSTIC KIDNEY DISEASE 1 | (OMIM:174000) |
NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE | (OMIM:310468) |
OCULORENOCEREBELLAR SYNDROME | (OMIM:257970) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Tyrosinemia type 1 | (Orphanet:882) |