Glomerulopathy
Symptom Information:
| Symptom ID: | HPO:0100820 | ||||
| Synonyms: |
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| Quality: | |||||
| 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) Glomerulopathy(HPO:0100820) MedDRA: |
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| Database Frequency: | 46 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Alport syndrome | (Orphanet:63) |
| Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis | (Orphanet:86818) |
| Alström syndrome | (Orphanet:64) |
| Anti-glomerular basement membrane disease | (Orphanet:375) |
| Behçet disease | (Orphanet:117) |
| Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
| Bullous impetigo | (Orphanet:36237) |
| CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
| Castleman disease | (Orphanet:160) |
| Cockayne syndrome | (Orphanet:191) |
| Cronkhite-Canada syndrome | (Orphanet:2930) |
| Cryoglobulinemic vasculitis | (Orphanet:91138) |
| Cystinosis | (Orphanet:213) |
| Dystrophic epidermolysis bullosa | (Orphanet:303) |
| Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
| Fabry disease | (Orphanet:324) |
| Familial LCAT deficiency | (Orphanet:79293) |
| Familial dysautonomia | (Orphanet:1764) |
| Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
| Fibronectin glomerulopathy | (Orphanet:84090) |
| Frasier syndrome | (Orphanet:347) |
| GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 | (OMIM:601894) |
| Granulomatosis with polyangiitis | (Orphanet:900) |
| Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | (Orphanet:324525) |
| Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
| Immunoglobulin A vasculitis | (Orphanet:761) |
| LCAT deficiency | (Orphanet:650) |
| Lipoprotein glomerulopathy | (Orphanet:329481) |
| Lymphedema - distichiasis | (Orphanet:33001) |
| MELAS | (Orphanet:550) |
| Majeed syndrome | (Orphanet:77297) |
| Maternally-inherited diabetes and deafness | (Orphanet:225) |
| Microcephaly - glomerulonephritis - marfanoid habitus | (Orphanet:2172) |
| Microscopic polyangiitis | (Orphanet:727) |
| Nail-patella syndrome | (Orphanet:2614) |
| Nail-patella-like renal disease | (Orphanet:2613) |
| Nephropathy - deafness - hyperparathyroidism | (Orphanet:2668) |
| Non-histaminic angioedema | (Orphanet:658) |
| Oculo-reno-cerebellar syndrome | (Orphanet:2715) |
| Oculocerebrorenal syndrome | (Orphanet:534) |
| Partial acquired lipodystrophy | (Orphanet:79087) |
| Prader-Willi syndrome | (Orphanet:739) |
| Relapsing polychondritis | (Orphanet:728) |
| Schimke immuno-osseous dysplasia | (Orphanet:1830) |
| Sweet syndrome | (Orphanet:3243) |
| Wiskott-Aldrich syndrome | (Orphanet:906) |