Chronic kidney disease

Symptom Information:

Symptom ID: HPO:0012622
Synonyms:
Loss of renal function [HPO:0012622]
Progressive renal failure [HPO:0012622]
Progressive renal insufficiency [HPO:0012622]
RENAL FAILURE, PROGRESSIVE [HPO:0012622]
Renal insufficiency, progressive [HPO:0012622]
Loss of renal function [OMIM:Loss of renal function]
Progressive renal failure [OMIM:Progressive renal failure]
Progressive renal insufficiency [OMIM:Progressive renal insufficiency]
Renal failure, progressive [OMIM:Renal failure, progressive]
Renal insufficiency, progressive [OMIM:Renal insufficiency, progressive]
Quality:
Cross references:
OMIM: "Loss of renal function" [OMIM:Loss of renal function]
OMIM: "Progressive renal failure" [OMIM:Progressive renal failure]
OMIM: "Progressive renal insufficiency" [OMIM:Progressive renal insufficiency]
OMIM: "Renal failure, progressive" [OMIM:Renal failure, progressive]
OMIM: "Renal insufficiency, progressive" [OMIM:Renal insufficiency, progressive]
Is a (Direct Parents):
HPO         Renal insufficiency
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:
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)