Stage 5 chronic kidney disease

Symptom Information:

Symptom ID: HPO:0003774
Synonyms:
Chronic renal failure [HPO:0003774]
End stage renal disease [HPO:0003774]
End stage renal failure [HPO:0003774]
End-stage renal disease [HPO:0003774]
End-stage renal failure [HPO:0003774]
RENAL FAILURE, ENDSTAGE [HPO:0003774]
Chronic renal failure [OMIM:Chronic renal failure]
End stage renal disease [OMIM:End stage renal disease]
End stage renal failure [OMIM:End stage renal failure]
End-stage renal disease [OMIM:End-stage renal disease]
End-stage renal failure [OMIM:End-stage renal failure]
Renal failure, endstage [OMIM:Renal failure, endstage]
End stage renal disease (20-40 years)(28% of patients) [OMIM:End stage renal disease (20-40 years)(28% of patients)]
End stage renal disease (33% of patients) [OMIM:End stage renal disease (33% of patients)]
End stage renal disease (age 6-35 years) [OMIM:End stage renal disease (age 6-35 years)]
End stage renal disease (seen in 20-40% of patients by 20 years after biopsy) [OMIM:End stage renal disease (seen in 20-40% of patients by 20 years after biopsy)]
End-stage renal disease (in some patients) [OMIM:End-stage renal disease (in some patients)]
End-stage renal disease (in some) [OMIM:End-stage renal disease (in some)]
End-stage renal failure (in some patients) [OMIM:End-stage renal failure (in some patients)]
Renal failure, chronic [OMIM:Renal failure, chronic]
Renal failure, endstage (in some patients) [OMIM:Renal failure, endstage (in some patients)]
Renal failure chronic [MedDRA:10038444]
Quality:
Cross references:
OMIM: "Chronic renal failure" [OMIM:Chronic renal failure]
OMIM: "End stage renal disease" [OMIM:End stage renal disease]
OMIM: "End stage renal failure" [OMIM:End stage renal failure]
OMIM: "End-stage renal disease" [OMIM:End-stage renal disease]
OMIM: "End-stage renal failure" [OMIM:End-stage renal failure]
OMIM: "Renal failure, endstage" [OMIM:Renal failure, endstage]
OMIM: "End stage renal disease (20-40 years)(28% of patients)" [OMIM:End stage renal disease (20-40 years)(28% of patients)]
OMIM: "End stage renal disease (33% of patients)" [OMIM:End stage renal disease (33% of patients)]
OMIM: "End stage renal disease (age 6-35 years)" [OMIM:End stage renal disease (age 6-35 years)]
OMIM: "End stage renal disease (seen in 20-40% of patients by 20 years after biopsy)" [OMIM:End stage renal disease (seen in 20-40% of patients by 20 years after biopsy)]
OMIM: "End-stage renal disease (in some patients)" [OMIM:End-stage renal disease (in some patients)]
OMIM: "End-stage renal disease (in some)" [OMIM:End-stage renal disease (in some)]
OMIM: "End-stage renal failure (in some patients)" [OMIM:End-stage renal failure (in some patients)]
OMIM: "Renal failure, chronic" [OMIM:Renal failure, chronic]
OMIM: "Renal failure, endstage (in some patients)" [OMIM:Renal failure, endstage (in some patients)]
Is a (Direct Parents):
MedDRA Renal failure and impairment
HPO         Chronic kidney disease
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)
                      Chronic kidney disease(HPO:0012622)
                         Stage 5 chronic kidney disease(HPO:0003774)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal physiology(HPO:0012211)
                      Renal insufficiency(HPO:0000083)
                         Chronic kidney disease(HPO:0012622)
                            Stage 5 chronic kidney disease(HPO:0003774)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
       Renal failure and impairment(MedDRA:10038443)
          Stage 5 chronic kidney disease(HPO:0003774)
Database Frequency: 78 / 7739
Resource:

All diseases associated with this symptom:

17q12 microdeletion syndrome (Orphanet:261265)
Alport syndrome (Orphanet:63)
Atypical hemolytic uremic syndrome with DGKE deficiency (Orphanet:357008)
Autosomal dominant Alport syndrome (Orphanet:88918)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E (Orphanet:93114)
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia (Orphanet:34149)
Autosomal dominant progressive nephropathy with hypertension (Orphanet:88659)
Autosomal recessive Alport syndrome (Orphanet:88919)
Autosomal recessive medullary cystic kidney disease (Orphanet:655)
BARTTER SYNDROME, TYPE 4A (OMIM:602522)
BARTTER SYNDROME, TYPE 4B (OMIM:613090)
Bardet-Biedl syndrome 16 (OMIM:615993)
C3 glomerulonephritis (Orphanet:329931)
CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT, SUSCEPTIBILITY TO (OMIM:610805)
CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE (OMIM:219900)
Cranioectodermal dysplasia 3 (OMIM:614099)
Cranioectodermal dysplasia 4 (OMIM:614378)
Denys-Drash syndrome (Orphanet:220)
EPSTEIN SYNDROME (OMIM:153650)
FANCONI ANEMIA, COMPLEMENTATION GROUP O (OMIM:613390)
FECHTNER SYNDROME (OMIM:153640)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO (OMIM:612551)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 7 (OMIM:616002)
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 8 (OMIM:616032)
Fabry disease (Orphanet:324)
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes (Orphanet:93216)
Fibronectin glomerulopathy (Orphanet:84090)
Frasier syndrome (Orphanet:347)
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 1 (OMIM:137950)
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (OMIM:601894)
INTERSTITIAL NEPHRITIS, KARYOMEGALIC (OMIM:614817)
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1 (OMIM:161950)
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2 (OMIM:613944)
Immunoglobulin-mediated membranoproliferative glomerulonephritis (Orphanet:329903)
Joubert syndrome 3 (OMIM:608629)
Joubert syndrome 5 (OMIM:610188)
Joubert syndrome 6 (OMIM:610688)
Joubert syndrome with ocular defect (Orphanet:220493)
Joubert syndrome with oculorenal defect (Orphanet:2318)
LAMB-2-related infantile-onset nephrotic syndrome (Orphanet:306507)
LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME (OMIM:308940)
Lysinuric protein intolerance (Orphanet:470)
NEPHROTIC SYNDROME, TYPE 3 (OMIM:610725)
NEPHROTIC SYNDROME, TYPE 9 (OMIM:615573)
Nephronophthisis 1 (OMIM:256100)
Nephronophthisis 12 (OMIM:613820)
Nephronophthisis 13 (OMIM:614377)
Nephronophthisis 14 (OMIM:614844)
Nephronophthisis 15 (OMIM:614845)
Nephronophthisis 16 (OMIM:615382)
Nephronophthisis 18 (OMIM:615862)
Nephronophthisis 19 (OMIM:616217)
Nephronophthisis 2 (OMIM:602088)
Nephronophthisis 3 (OMIM:604387)
Nephronophthisis 4 (OMIM:606966)
Nephronophthisis 7 (OMIM:611498)
Nephronophthisis 9 (OMIM:613824)
Nephronophthisis-like nephropathy 1 (OMIM:613159)
Nephrotic syndrome-deafness-pretibial epidermolysis bullosa syndrome (Orphanet:300333)
Pierson syndrome (Orphanet:2670)
Primary hyperoxaluria type 1 (Orphanet:93598)
Renal coloboma syndrome (Orphanet:1475)
Renal cysts and diabetes syndrome (Orphanet:93111)
Saldino-Mainzer syndrome (Orphanet:140969)
Senior-Boichis syndrome (Orphanet:84081)
Senior-Loken syndrome (Orphanet:3156)
Senior-Loken syndrome 1 (OMIM:266900)
Senior-Loken syndrome 3 (OMIM:606995)
Senior-Loken syndrome 4 (OMIM:606996)
Senior-Loken syndrome 5 (OMIM:609254)
Senior-Loken syndrome 6 (OMIM:610189)
Senior-Loken syndrome 9 (OMIM:616629)
Short-rib thoracic dysplasia 5 with or without polydactyly (OMIM:614376)
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)
Wolfram syndrome 2 (OMIM:604928)
X-linked Alport syndrome (Orphanet:88917)