Renal insufficiency

Symptom Information:

Symptom ID: HPO:0000083
Synonyms:
Renal failure [HPO:0000083]
Renal failure in adulthood [HPO:0000083]
Renal failure [Orphanet:38200]
Renal failure syndrome (disorder) [Orphanet:38200]
Renal impairment (disorder) [Orphanet:38200]
Kidney Failure [Orphanet:38200]
Renal impairment [Orphanet:38200]
Renal failure [OMIM:Renal failure]
Renal failure in adulthood [OMIM:Renal failure in adulthood]
Renal insufficiency [OMIM:Renal insufficiency]
Renal failure [MedDRA:10038435]
Failure kidney [MedDRA:10038435]
Insufficiency renal [MedDRA:10038435]
Kidney failure [MedDRA:10038435]
Progressive renal failure [MedDRA:10038435]
Renal failure aggravated [MedDRA:10038435]
Renal failure following abortion and ectopic and molar pregnancies [MedDRA:10038435]
Renal failure NOS [MedDRA:10038435]
Renal failure unspecified [MedDRA:10038435]
Renal failure, unspecified [MedDRA:10038435]
Renal insufficiency [MedDRA:10038435]
Renal insufficiency aggravated [MedDRA:10038435]
Anuric renal failure [MedDRA:10038435]
Renal impairment [MedDRA:10062237]
Chronic renal impairment [MedDRA:10062237]
Disorders resulting from impaired renal function [MedDRA:10062237]
Dysfunction kidney [MedDRA:10062237]
Function kidney abnormal [MedDRA:10062237]
Function kidney decreased [MedDRA:10062237]
Impaired renal function [MedDRA:10062237]
Kidney dysfunction [MedDRA:10062237]
Kidney function abnormal [MedDRA:10062237]
Other specified disorders resulting from impaired renal function [MedDRA:10062237]
Renal function abnormal [MedDRA:10062237]
Renal function abnormal glomer [MedDRA:10062237]
Renal function aggravated [MedDRA:10062237]
Renal function disorder [MedDRA:10062237]
Renal impairment NOS [MedDRA:10062237]
Unspecified disorder resulting from impaired renal function [MedDRA:10062237]
Abnormal renal function [OMIM:Abnormal renal function]
Impaired renal function (variable) [OMIM:Impaired renal function (variable)]
Renal failure (in some patients) [OMIM:Renal failure (in some patients)]
Renal failure (most common cause of death) (Iowa type 107680.0010) [OMIM:Renal failure (most common cause of death) (Iowa type 107680.0010)]
Renal insufficiency (in 2 of 3 siblings) [OMIM:Renal insufficiency (in 2 of 3 siblings)]
Renal insufficiency (in some patients) [OMIM:Renal insufficiency (in some patients)]
Quality:
Cross references:
Orphanet:38200 "Renal failure" [Orphanet:38200]
OMIM: "Renal failure" [OMIM:Renal failure]
OMIM: "Renal failure in adulthood" [OMIM:Renal failure in adulthood]
OMIM: "Renal insufficiency" [OMIM:Renal insufficiency]
OMIM: "Abnormal renal function" [OMIM:Abnormal renal function]
OMIM: "Impaired renal function (variable)" [OMIM:Impaired renal function (variable)]
OMIM: "Renal failure (in some patients)" [OMIM:Renal failure (in some patients)]
OMIM: "Renal failure (most common cause of death) (Iowa type 107680.0010)" [OMIM:Renal failure (most common cause of death) (Iowa type 107680.0010)]
OMIM: "Renal insufficiency (in 2 of 3 siblings)" [OMIM:Renal insufficiency (in 2 of 3 siblings)]
OMIM: "Renal insufficiency (in some patients)" [OMIM:Renal insufficiency (in some patients)]
UMLS:C0035078 "Kidney Failure" [Orphanet:38200]
UMLS:C0341697 "Renal impairment" [Orphanet:38200]
Is a (Direct Parents):
MedDRA Renal failure and impairment
HPO         Abnormal renal physiology
Orphanet Nephropathy
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)
                      Renal insufficiency(HPO:0000083)
             Abnormality of the urinary system physiology(HPO:0011277)
                Abnormal renal physiology(HPO:0012211)
                   Renal insufficiency(HPO:0000083)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
       Renal failure and impairment(MedDRA:10038443)
          Renal insufficiency(HPO:0000083)
Database Frequency: 232 / 7739
Resource:

All diseases associated with this symptom:

17q12 microdeletion syndrome (Orphanet:261265)
ACRORENAL SYNDROME, AUTOSOMAL RECESSIVE (OMIM:201310)
APOLIPOPROTEIN A-I (OMIM:107680)
ARIMA SYNDROME (OMIM:243910)
ATTRV122I amyloidosis (Orphanet:85451)
Acquired ichthyosis (Orphanet:454)
Acrorenal syndrome (Orphanet:971)
Action myoclonus - renal failure syndrome (Orphanet:163696)
Acute intermittent porphyria (Orphanet:79276)
Acyl-CoA dehydrogenase 9 deficiency (Orphanet:99901)
Adenine phosphoribosyltransferase deficiency (Orphanet:976)
Adult familial nephronophtisis - spastic quadriparesia (Orphanet:2666)
Alagille syndrome due to a NOTCH2 point mutation (Orphanet:261629)
Alport syndrome (Orphanet:63)
Alport syndrome - intellectual deficit - midface hypoplasia - elliptocytosis (Orphanet:86818)
Alström syndrome (Orphanet:64)
Amelogenesis imperfecta - nephrocalcinosis (Orphanet:1031)
Anti-glomerular basement membrane disease (Orphanet:375)
Arthrogryposis due to muscular dystrophy (Orphanet:1155)
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures (Orphanet:73229)
Autosomal dominant progressive nephropathy with hypertension (Orphanet:88659)
Autosomal recessive medullary cystic kidney disease (Orphanet:655)
Autosomal recessive polycystic kidney disease (Orphanet:731)
BARTTER SYNDROME, TYPE 4B (OMIM:613090)
BOR syndrome (Orphanet:107)
BRACHYMESOMELIA-RENAL SYNDROME (OMIM:113470)
BRANCHIOOTORENAL SYNDROME 2 (OMIM:610896)
Babesiosis (Orphanet:108)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 17 (OMIM:615994)
Bardet-Biedl syndrome 18 (OMIM:615995)
Bardet-Biedl syndrome 19 (OMIM:615996)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 8 (OMIM:615985)
Behçet disease (Orphanet:117)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Blau syndrome (Orphanet:90340)
Blue diaper syndrome (Orphanet:94086)
C3 glomerulonephritis (Orphanet:329931)
COCKAYNE SYNDROME A (OMIM:216400)
COCKAYNE SYNDROME B (OMIM:133540)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Carnitine palmitoyl transferase II deficiency (Orphanet:157)
Carnitine palmitoyl transferase II deficiency, myopathic form (Orphanet:228302)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
Castleman disease (Orphanet:160)
Caudal regression sequence (Orphanet:3027)
Cerebro-reno-digital syndrome (Orphanet:1396)
Chronic hiccup (Orphanet:396)
Cirrhotic cardiomyopathy (Orphanet:57777)
Cockayne syndrome (Orphanet:191)
Complement component 3 deficiency (Orphanet:280133)
Congenital intrauterine infection-like syndrome (Orphanet:1229)
Congenital nephrotic syndrome, Finnish type (Orphanet:839)
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome (Orphanet:306504)
Cornelia de Lange syndrome (Orphanet:199)
Costello syndrome (Orphanet:3071)
Cryoglobulinemic vasculitis (Orphanet:91138)
Cystinosis (Orphanet:213)
Cystinuria (Orphanet:214)
Cystinuria type A (Orphanet:93612)
Cystinuria type B (Orphanet:93613)
DK1-CDG (Orphanet:91131)
Dahlberg-Borer-Newcomer syndrome (Orphanet:1563)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
Dent disease type 1 (Orphanet:93622)
Dent disease type 2 (Orphanet:93623)
Diffuse cutaneous systemic sclerosis (Orphanet:220393)
Diffuse neonatal hemangiomatosis (Orphanet:2123)
Distal limb deficiencies - micrognathia syndrome (Orphanet:1307)
Drug rash with eosinophilia and systemic symptoms (Orphanet:139402)
Dystrophic epidermolysis bullosa (Orphanet:303)
Ebola hemorrhagic fever (Orphanet:319218)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Erdheim-Chester disease (Orphanet:35687)
FAMILIAL MEDITERRANEAN FEVER (OMIM:249100)
FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT (OMIM:134610)
FANCONI RENOTUBULAR SYNDROME 2 (OMIM:613388)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO (OMIM:607832)
Fabry disease (Orphanet:324)
Familial LCAT deficiency (Orphanet:79293)
Familial Mediterranean fever (Orphanet:342)
Familial amyloidosis, Finnish type (Orphanet:85448)
Familial dysautonomia (Orphanet:1764)
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis (Orphanet:31043)
Familial idiopathic steroid-resistant nephrotic syndrome (Orphanet:656)
Familial juvenile hyperuricemic nephropathy type 1 (Orphanet:209886)
Fanconi anemia (Orphanet:84)
Fanconi renotubular syndrome 1 (OMIM:134600)
Fibronectin glomerulopathy (Orphanet:84090)
Frasier syndrome (Orphanet:347)
GLOMERULOCYSTIC KIDNEY DISEASE WITH HYPERURICEMIA AND ISOSTHENURIA (OMIM:609886)
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1 (OMIM:137950)
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (OMIM:601894)
GLYCOGEN STORAGE DISEASE Ic (OMIM:232240)
Galactosemia (Orphanet:352)
Giant cell arteritis (Orphanet:397)
Glomerulonephritis - sparse hair - telangiectasis (Orphanet:2087)
Glycogen storage disease due to glucose-6-phosphatase deficiency type a (Orphanet:79258)
Glycogen storage disease due to glucose-6-phosphatase deficiency type b (Orphanet:79259)
Glycogen storage disease due to lactate dehydrogenase deficiency (Orphanet:2364)
Glycogen storage disease due to muscle glycogen phosphorylase deficiency (Orphanet:368)
Glycogen storage disease due to phosphoglycerate kinase 1 deficiency (Orphanet:713)
Glycogen storage disease due to phosphoglycerate mutase deficiency (Orphanet:97234)
Granulomatosis with polyangiitis (Orphanet:900)
HERMANSKY-PUDLAK SYNDROME 1 (OMIM:203300)
HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3 (OMIM:614227)
HYPERVITAMINOSIS A, SUSCEPTIBILITY TO (OMIM:240150)
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE (OMIM:300554)
Hairy cell leukemia variant (Orphanet:300878)
Hand-foot-genital syndrome (Orphanet:2438)
Hemorrhagic fever - renal syndrome (Orphanet:340)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hermansky-Pudlak syndrome with pulmonary fibrosis (Orphanet:231500)
Hinman syndrome (Orphanet:84085)
Holoprosencephaly - caudal dysgenesis (Orphanet:2165)
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation (Orphanet:324525)
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome (Orphanet:363694)
Hypocomplementemic urticarial vasculitis (Orphanet:36412)
Hypoparathyroidism - deafness - renal disease (Orphanet:2237)
Immunodeficiency with factor I anomaly (Orphanet:200418)
Immunoglobulin A vasculitis (Orphanet:761)
Indomethacin embryofetopathy (Orphanet:1909)
Infantile Bartter syndrome with deafness (Orphanet:89938)
Jeune syndrome (Orphanet:474)
Joubert syndrome 2 (OMIM:608091)
Joubert syndrome 4 (OMIM:609583)
Joubert syndrome with hepatic defect (Orphanet:1454)
Joubert syndrome with oculorenal defect (Orphanet:2318)
Joubert syndrome with renal defect (Orphanet:220497)
Junctional epidermolysis bullosa (Orphanet:305)
Kelley-Seegmiller syndrome (Orphanet:79233)
Kleefstra syndrome (Orphanet:261494)
Kleefstra syndrome due to 9q34 microdeletion (Orphanet:96147)
LCAT deficiency (Orphanet:650)
Lamellar ichthyosis (Orphanet:313)
Laurence-Moon syndrome (Orphanet:2377)
Legionellosis (Orphanet:549)
Lesch-Nyhan syndrome (Orphanet:510)
Liddle syndrome (Orphanet:526)
Limited cutaneous systemic sclerosis (Orphanet:220402)
Limited systemic sclerosis (Orphanet:220407)
Lipoprotein glomerulopathy (Orphanet:329481)
Lyell syndrome (Orphanet:537)
MELAS (Orphanet:550)
MESANGIAL SCLEROSIS, DIFFUSE RENAL, WITH OCULAR ABNORMALITIES (OMIM:249660)
Maternally-inherited diabetes and deafness (Orphanet:225)
McKusick-Kaufman syndrome (Orphanet:2473)
Methylmalonic acidemia with homocystinuria, type cblC (Orphanet:79282)
Methylmalonic acidemia without homocystinuria (Orphanet:293355)
Microcephaly - glomerulonephritis - marfanoid habitus (Orphanet:2172)
Microscopic polyangiitis (Orphanet:727)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Muckle-Wells syndrome (Orphanet:575)
Mulibrey nanism (Orphanet:2576)
Multicentric carpo-tarsal osteolysis with or without nephropathy (Orphanet:2774)
Multicystic renal dysplasia (Orphanet:1851)
NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE (OMIM:310468)
NEPHROSIALIDOSIS (OMIM:256150)
NEPHROTIC SYNDROME, TYPE 4 (OMIM:256370)
Nail-patella syndrome (Orphanet:2614)
Nail-patella-like renal disease (Orphanet:2613)
Neonatal hemochromatosis (Orphanet:446)
Nephronophthisis 16 (OMIM:615382)
Nephronophthisis 3 (OMIM:604387)
Nephropathy - deafness - hyperparathyroidism (Orphanet:2668)
Nephrosis - deafness - urinary tract - digital malformations (Orphanet:2669)
Ochoa syndrome (Orphanet:2704)
Oculo-reno-cerebellar syndrome (Orphanet:2715)
Oculo-skeletal-renal syndrome (Orphanet:2716)
Oculocerebrorenal syndrome (Orphanet:534)
Orofaciodigital syndrome type 1 (Orphanet:2750)
POLYCYSTIC KIDNEY DISEASE 1 (OMIM:173900)
POLYCYSTIC KIDNEY DISEASE 2 (OMIM:613095)
PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS (OMIM:308990)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Phosphoribosylpyrophosphate synthetase superactivity (Orphanet:3222)
Polyarteritis nodosa (Orphanet:767)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Primary Fanconi syndrome (Orphanet:3337)
Primary hyperoxaluria (Orphanet:416)
Primary hyperoxaluria type 1 (Orphanet:93598)
Primary hyperoxaluria type 2 (Orphanet:93599)
Primary hyperoxaluria type 3 (Orphanet:93600)
Prune belly syndrome (Orphanet:2970)
Pyomyositis (Orphanet:764)
Pyruvate carboxylase deficiency (Orphanet:3008)
RENAL DYSPLASIA, CYSTIC, SUSCEPTIBILITY TO (OMIM:601331)
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
RHYNS syndrome (Orphanet:140976)
Recessive dystrophic epidermolysis bullosa inversa (Orphanet:79409)
Refsum disease (Orphanet:773)
Relapsing polychondritis (Orphanet:728)
Renal coloboma syndrome (Orphanet:1475)
Renal cysts and diabetes syndrome (Orphanet:93111)
Renal-hepatic-pancreatic dysplasia (Orphanet:294415)
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications (Orphanet:3018)
Scalp-ear-nipple syndrome (Orphanet:2036)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Scleroderma (Orphanet:801)
Scrub typhus (Orphanet:83317)
Senior-Loken syndrome 1 (OMIM:266900)
Senior-Loken syndrome 7 (OMIM:613615)
Short-rib thoracic dysplasia 1 with or without polydactyly (OMIM:208500)
Sialidosis type 2 (Orphanet:87876)
Siegler-Brewer-Carey syndrome (Orphanet:3167)
Stevens-Johnson syndrome (Orphanet:36426)
Sweet syndrome (Orphanet:3243)
Syndactyly - telecanthus - anogenital and renal malformations (Orphanet:140952)
Syndromic X-linked ichthyosis (Orphanet:281090)
Systemic capillary leak syndrome (Orphanet:188)
Thyrocerebrorenal syndrome (Orphanet:3327)
Torticollis - keloids - cryptorchidism - renal dysplasia (Orphanet:3341)
Townes-Brocks syndrome (Orphanet:857)
Tuberous sclerosis (Orphanet:805)
Tyrosinemia type 1 (Orphanet:882)
UROFACIAL SYNDROME 2 (OMIM:615112)
VENTRICULOMEGALY WITH CYSTIC KIDNEY DISEASE (OMIM:219730)
Vitamin B12-responsive methylmalonic acidemia (Orphanet:28)
Vitamin B12-unresponsive methylmalonic acidemia (Orphanet:27)
Vitamin B12-unresponsive methylmalonic acidemia type mut- (Orphanet:79312)
Vitamin B12-unresponsive methylmalonic acidemia type mut0 (Orphanet:289916)
WAGR syndrome (Orphanet:893)
WILMS TUMOR, ANIRIDIA, GENITOURINARY ANOMALIES, AND MENTAL RETARDATIONSYNDROME (OMIM:194072)
Waldenström macroglobulinemia (Orphanet:33226)
Williams syndrome (Orphanet:904)
Wilson disease (Orphanet:905)
Wolcott-Rallison syndrome (Orphanet:1667)
Wolfram syndrome 2 (OMIM:604928)
Yellow fever (Orphanet:99829)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)
[DEL] PSEUDOXANTHOMA ELASTICUM (OMIM:264800)