Decreased glomerular filtration rate
Symptom Information:
Symptom ID: | HPO:0012213 | ||||||||
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) 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) |
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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) |