Renal insufficiency
Symptom Information:
Symptom ID: | HPO:0000083 | |||||||||||||||||||||||||||||||||||||||||||||
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 urinary system physiology(HPO:0011277) Abnormal renal physiology(HPO:0012211) Renal insufficiency(HPO:0000083) Abnormality of the upper urinary tract(HPO:0010935) Abnormality of the kidney(HPO:0000077) 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) |
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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) |