Nephropathy

Symptom Information:

Symptom ID: HPO:0000112
Synonyms:
Kidney disease [Orphanet:38040]
Kidney disease (disorder) [Orphanet:38040]
Kidney Diseases [Orphanet:38040]
Nephropathy [OMIM:Nephropathy]
Renal disease/nephropathy [Orphanet:38040]
Nephropathy [Orphanet:38040]
Renal disorder [Orphanet:38040]
Nephropathy [MedDRA:10029151]
Nephropathy NOS [MedDRA:10029151]
Renal disease [MedDRA:10029151]
Renal disorder [MedDRA:10038428]
Disorder kidney [MedDRA:10038428]
Disorder renal [MedDRA:10038428]
Other disorders of kidney and ureter [MedDRA:10038428]
Other specified disorder of kidney and ureter [MedDRA:10038428]
Other specified disorders of kidney and ureter [MedDRA:10038428]
Renal disorder NOS [MedDRA:10038428]
Unspecified disorder of kidney and ureter [MedDRA:10038428]
Kidney disorder [MedDRA:10038428]
Renal disease [OMIM:Renal disease]
Nephropathies [MedDRA:10029149]
Renal disorders (excl nephropathies) [MedDRA:10038430]
Quality:
Cross references:
HPO:0000082 "Abnormality of renal physiology" [Orphanet:38040]
Orphanet:38040 "Renal disease/nephropathy" [Orphanet:38040]
OMIM: "Nephropathy" [OMIM:Nephropathy]
OMIM: "Renal disease" [OMIM:Renal disease]
UMLS:C0022658 "Kidney Diseases" [Orphanet:38040]
Is a (Direct Parents):
Orphanet Abnormality of the urinary system physiology
MedDRA Renal and urinary disorders
MedDRA Nephropathies and tubular disorders NEC
MedDRA Renal disorders NEC
HPO         Abnormal renal physiology
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 urinary system physiology(HPO:0011277)
                Abnormal renal physiology(HPO:0012211)
                   Nephropathy(HPO:0000112)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal physiology(HPO:0012211)
                      Nephropathy(HPO:0000112)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
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)