Nephropathy
Symptom Information:
Symptom ID: | HPO:0000112 | ||||||||||||||||||||||
Synonyms: |
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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 physiology(HPO:0012211) Nephropathy(HPO:0000112) Abnormality of the urinary system physiology(HPO:0011277) Abnormal renal physiology(HPO:0012211) Nephropathy(HPO:0000112) MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) |
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Database Frequency: | 92 / 7739 | ||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ALG1-CDG | (Orphanet:79327) |
ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2 | (OMIM:613404) |
Action myoclonus - renal failure syndrome | (Orphanet:163696) |
Adenine phosphoribosyltransferase deficiency | (Orphanet:976) |
Alström syndrome | (Orphanet:64) |
Amelogenesis imperfecta - nephrocalcinosis | (Orphanet:1031) |
Antecubital pterygium syndrome | (Orphanet:2987) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy | (Orphanet:1192) |
Autosomal dominant beta2-microglobulinic amyloidosis | (Orphanet:314652) |
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures | (Orphanet:73229) |
Beckwith-Wiedemann syndrome | (Orphanet:116) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Blau syndrome | (Orphanet:90340) |
Cerebroretinal vasculopathy | (Orphanet:3421) |
Congenital disorder of glycosylation | (Orphanet:137) |
Cranioectodermal dysplasia 4 | (OMIM:614378) |
Cystinosis | (Orphanet:213) |
DANUBIAN ENDEMIC FAMILIAL NEPHROPATHY | (OMIM:124100) |
Dahlberg-Borer-Newcomer syndrome | (Orphanet:1563) |
Denys-Drash syndrome | (Orphanet:220) |
Dyschondrosteosis - nephritis | (Orphanet:1765) |
Fabry disease | (Orphanet:324) |
Familial Mediterranean fever | (Orphanet:342) |
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement | (Orphanet:2196) |
Familial isolated hypoparathyroidism | (Orphanet:2238) |
Familial juvenile hyperuricemic nephropathy type 1 | (Orphanet:209886) |
Fibronectin glomerulopathy | (Orphanet:84090) |
Galloway-Mowat syndrome | (Orphanet:2065) |
HERNS syndrome | (Orphanet:63261) |
HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3 | (OMIM:614227) |
Hereditary vascular retinopathy | (Orphanet:71291) |
Hydrocephalus - blue sclerae - nephropathy | (Orphanet:2186) |
Hyperprolinemia type 1 | (Orphanet:419) |
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | (Orphanet:324525) |
Ichthyosis - intellectual deficit - dwarfism - renal impairment | (Orphanet:2278) |
Indomethacin embryofetopathy | (Orphanet:1909) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
Ito hypomelanosis | (Orphanet:435) |
Jeune syndrome | (Orphanet:474) |
Joubert syndrome with hepatic defect | (Orphanet:1454) |
Joubert syndrome with oculorenal defect | (Orphanet:2318) |
Joubert syndrome with renal defect | (Orphanet:220497) |
LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME | (OMIM:308940) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Leigh syndrome with nephrotic syndrome | (Orphanet:255249) |
Liddle syndrome | (Orphanet:526) |
Lowe-Kohn-Cohen syndrome | (Orphanet:2408) |
MELAS | (Orphanet:550) |
Madelung deformity | (Orphanet:35688) |
Maturity-onset diabetes of the young, type 6 | (OMIM:606394) |
Methylmalonic acidemia with homocystinuria, type cblC | (Orphanet:79282) |
Miller-Dieker syndrome | (Orphanet:531) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Mixed connective tissue disease | (Orphanet:809) |
Mu heavy-chain disease | (Orphanet:100024) |
Muckle-Wells syndrome | (Orphanet:575) |
Multicentric carpo-tarsal osteolysis with or without nephropathy | (Orphanet:2774) |
Nail-patella syndrome | (Orphanet:2614) |
Nail-patella-like renal disease | (Orphanet:2613) |
Nephropathy - deafness - hyperparathyroidism | (Orphanet:2668) |
Nephrotic syndrome-deafness-pretibial epidermolysis bullosa syndrome | (Orphanet:300333) |
OCULORENOCEREBELLAR SYNDROME | (OMIM:257970) |
PHOTOMYOCLONUS, DIABETES MELLITUS, DEAFNESS, NEPHROPATHY, AND CEREBRALDYSFUNCTION | (OMIM:172500) |
POEMS syndrome | (Orphanet:2905) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Pendred syndrome | (Orphanet:705) |
Polyarteritis nodosa | (Orphanet:767) |
Primary hyperoxaluria | (Orphanet:416) |
Primary sclerosing cholangitis | (Orphanet:171) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Renal tubular dysgenesis | (Orphanet:3033) |
Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Saldino-Mainzer syndrome | (Orphanet:140969) |
Scleroderma | (Orphanet:801) |
Sialidosis type 2 | (Orphanet:87876) |
Sneddon syndrome | (Orphanet:820) |
Spastic paraplegia - nephritis - deafness | (Orphanet:2820) |
THROMBOCYTOPENIA WITH ELEVATED SERUM IgA AND RENAL DISEASE | (OMIM:314000) |
TRAPS syndrome | (Orphanet:32960) |
Torticollis - keloids - cryptorchidism - renal dysplasia | (Orphanet:3341) |
Very long chain acyl-CoA dehydrogenase deficiency | (Orphanet:26793) |
WAGR syndrome | (Orphanet:893) |
WISKOTT-ALDRICH SYNDROME | (OMIM:301000) |
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM | (OMIM:600903) |
Wiskott-Aldrich syndrome | (Orphanet:906) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
Wolfram syndrome | (Orphanet:3463) |
Yellow fever | (Orphanet:99829) |
[DEL] ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1 | (OMIM:208085) |