Tubular atrophy
Symptom Information:
| Symptom ID: | HPO:0000092 | ||
| 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 renal tubule(HPO:0000091) Tubular atrophy(HPO:0000092) MedDRA: |
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| Database Frequency: | 28 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| ARIMA SYNDROME | (OMIM:243910) |
| Alström syndrome | (Orphanet:64) |
| Autosomal dominant medullary cystic kidney disease with or without hyperuricemia | (Orphanet:34149) |
| Autosomal recessive medullary cystic kidney disease | (Orphanet:655) |
| Congenital nephrotic syndrome, Finnish type | (Orphanet:839) |
| Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome | (Orphanet:306504) |
| Dent disease type 1 | (Orphanet:93622) |
| FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6 | (OMIM:614131) |
| Fabry disease | (Orphanet:324) |
| Familial juvenile hyperuricemic nephropathy type 1 | (Orphanet:209886) |
| Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | (Orphanet:324525) |
| Hyperuricemia - anemia - renal failure | (Orphanet:217330) |
| Joubert syndrome with oculorenal defect | (Orphanet:2318) |
| MEDULLARY CYSTIC KIDNEY DISEASE 1 | (OMIM:174000) |
| NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE | (OMIM:310468) |
| Nephronophthisis 1 | (OMIM:256100) |
| Nephronophthisis 12 | (OMIM:613820) |
| Nephronophthisis 18 | (OMIM:615862) |
| Nephronophthisis 2 | (OMIM:602088) |
| Nephronophthisis 3 | (OMIM:604387) |
| Nephronophthisis 4 | (OMIM:606966) |
| Nephronophthisis 7 | (OMIM:611498) |
| Nephronophthisis-like nephropathy 1 | (OMIM:613159) |
| PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS | (OMIM:308990) |
| Primary Fanconi syndrome | (Orphanet:3337) |
| Proximal renal tubular acidosis | (Orphanet:47159) |
| Senior-Boichis syndrome | (Orphanet:84081) |
| Senior-Loken syndrome 6 | (OMIM:610189) |