Decreased glomerular filtration rate

Symptom Information:

Symptom ID: HPO:0012213
Synonyms:
Impaired renal creatinine clearance [HPO:0012213]
Reduced creatinine clearance [HPO:0012213]
Decreased glomerular filtration rate [OMIM:Decreased glomerular filtration rate]
Impaired renal creatinine clearance [OMIM:Impaired renal creatinine clearance]
Reduced creatinine clearance [OMIM:Reduced creatinine clearance]
Decreased glomerular filtration rate (GFR) [OMIM:Decreased glomerular filtration rate (GFR)]
Glomerular filtration rate, decreased [OMIM:Glomerular filtration rate, decreased]
Glomerular filtration rate decreased [MedDRA:10018358]
Quality:
Cross references:
OMIM: "Decreased glomerular filtration rate" [OMIM:Decreased glomerular filtration rate]
OMIM: "Impaired renal creatinine clearance" [OMIM:Impaired renal creatinine clearance]
OMIM: "Reduced creatinine clearance" [OMIM:Reduced creatinine clearance]
OMIM: "Decreased glomerular filtration rate (GFR)" [OMIM:Decreased glomerular filtration rate (GFR)]
OMIM: "Glomerular filtration rate, decreased" [OMIM:Glomerular filtration rate, decreased]
Is a (Direct Parents):
HPO         Abnormal glomerular filtration rate
MedDRA Renal function analyses
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)
                   Abnormal glomerular filtration rate(HPO:0012212)
                      Decreased glomerular filtration rate(HPO:0012213)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal physiology(HPO:0012211)
                      Abnormal glomerular filtration rate(HPO:0012212)
                         Decreased glomerular filtration rate(HPO:0012213)
MedDRA:
Investigations(MedDRA:10022891)
    Renal and urinary tract investigations and urinalyses(MedDRA:10038362)
       Renal function analyses(MedDRA:10038454)
          Decreased glomerular filtration rate(HPO:0012213)
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures (Orphanet:73229)
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia (Orphanet:34149)
BARTTER SYNDROME, TYPE 4A (OMIM:602522)
BARTTER SYNDROME, TYPE 4B (OMIM:613090)
CYSTINOSIS, NEPHROPATHIC (OMIM:219800)
Cystinosis (Orphanet:213)
Dent disease type 1 (Orphanet:93622)
Dent disease type 2 (Orphanet:93623)
FANCONI RENOTUBULAR SYNDROME 2 (OMIM:613388)
Fabry disease (Orphanet:324)
GLYCOGEN STORAGE DISEASE Ic (OMIM:232240)
Glycogen storage disease due to glucose-6-phosphatase deficiency (Orphanet:364)
Glycogen storage disease due to glucose-6-phosphatase deficiency type a (Orphanet:79258)
Ichthyosis - intellectual deficit - dwarfism - renal impairment (Orphanet:2278)
Infantile Bartter syndrome with deafness (Orphanet:89938)
MEDULLARY CYSTIC KIDNEY DISEASE 1 (OMIM:174000)
Primary hyperoxaluria type 3 (Orphanet:93600)
Renal cysts and diabetes syndrome (Orphanet:93111)
Sneddon syndrome (Orphanet:820)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)