Stage 5 chronic kidney disease
Symptom Information:
Symptom ID: | HPO:0003774 | ||||||||||||||||||||||
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) 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) |
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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) |