Nephritis
Symptom Information:
| Symptom ID: | HPO:0000123 | ||||||
| Synonyms: |
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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 urinary system physiology(HPO:0011277) Abnormal renal physiology(HPO:0012211) Nephritis(HPO:0000123) Abnormality of the upper urinary tract(HPO:0010935) Abnormality of the kidney(HPO:0000077) Abnormal renal physiology(HPO:0012211) Nephritis(HPO:0000123) MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Nephritis NEC(MedDRA:10029137) Nephritis(HPO:0000123) |
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| Database Frequency: | 18 / 7739 | ||||||
| Resource: |
All diseases associated with this symptom:
| AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA | (OMIM:603909) |
| Alström syndrome | (Orphanet:64) |
| Autosomal dominant progressive nephropathy with hypertension | (Orphanet:88659) |
| Autosomal recessive Alport syndrome | (Orphanet:88919) |
| Autosomal recessive systemic lupus erythematosus | (Orphanet:300345) |
| COMPLEMENT COMPONENT C1r/C1s DEFICIENCY | (OMIM:216950) |
| Dyschondrosteosis - nephritis | (Orphanet:1765) |
| EPSTEIN SYNDROME | (OMIM:153650) |
| FECHTNER SYNDROME | (OMIM:153640) |
| Hypoplasminogenemia | (Orphanet:722) |
| IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1 | (OMIM:161950) |
| Nephrotic syndrome-deafness-pretibial epidermolysis bullosa syndrome | (Orphanet:300333) |
| Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
| RETINAL VENOUS BEADING | (OMIM:180080) |
| SYSTEMIC LUPUS ERYTHEMATOSUS | (OMIM:152700) |
| Thyrocerebrorenal syndrome | (Orphanet:3327) |
| Torticollis - keloids - cryptorchidism - renal dysplasia | (Orphanet:3341) |
| X-linked Alport syndrome | (Orphanet:88917) |