Chronic kidney disease
Symptom Information:
Symptom ID: | HPO:0012622 | ||||||||||
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 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) Abnormality of the urinary system physiology(HPO:0011277) Abnormal renal physiology(HPO:0012211) Renal insufficiency(HPO:0000083) Chronic kidney disease(HPO:0012622) MedDRA: |
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Database Frequency: | 32 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
ARTERIOSCLEROSIS, SEVERE JUVENILE | (OMIM:208060) |
Autosomal dominant progressive nephropathy with hypertension | (Orphanet:88659) |
Bardet-Biedl syndrome 2 | (OMIM:615981) |
Cranioectodermal dysplasia | (Orphanet:1515) |
Cranioectodermal dysplasia 1 | (OMIM:218330) |
Cryoglobulinemic vasculitis | (Orphanet:91138) |
Cystinuria | (Orphanet:214) |
Dense deposit disease | (Orphanet:93571) |
Dent disease type 1 | (Orphanet:93622) |
Dent disease type 2 | (Orphanet:93623) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2 | (OMIM:603965) |
FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6 | (OMIM:614131) |
Fabry disease | (Orphanet:324) |
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis | (Orphanet:31043) |
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement | (Orphanet:2196) |
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE | (OMIM:300554) |
Hyperuricemia - anemia - renal failure | (Orphanet:217330) |
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome | (Orphanet:363694) |
Hypoparathyroidism - deafness - renal disease | (Orphanet:2237) |
Immunodeficiency with factor H anomaly | (Orphanet:200421) |
Jeune syndrome | (Orphanet:474) |
Joubert syndrome 5 | (OMIM:610188) |
MELAS | (Orphanet:550) |
NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE | (OMIM:310468) |
NEPHROPATHY, PROGRESSIVE TUBULOINTERSTITIAL, WITH CHOLESTATIC LIVERDISEASE | (OMIM:602114) |
NEPHROTIC SYNDROME, TYPE 8 | (OMIM:615244) |
Primary sclerosing cholangitis | (Orphanet:171) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Senior-Loken syndrome 6 | (OMIM:610189) |
Short-rib thoracic dysplasia 10 with or without polydactyly | (OMIM:615630) |
Vitamin B12-unresponsive methylmalonic acidemia type mut0 | (Orphanet:289916) |
Wolfram syndrome 1 | (OMIM:222300) |