Abnormal renal physiology

Symptom Information:

Symptom ID: HPO:0012211
Synonyms:
Abnormality of renal physiology [HPO:0012211]
Decreased renal function [HPO:0012211]
Impaired renal function [HPO:0012211]
Loss of renal function [HPO:0012211]
Reduced renal function [HPO:0012211]
Renal dysfunction [HPO:0012211]
Renal functional abnormality [HPO:0012211]
Decreased renal function [OMIM:Decreased renal function]
Impaired renal function [OMIM:Impaired renal function]
Renal dysfunction [OMIM:Renal dysfunction]
Impaired renal function (variable) [OMIM:Impaired renal function (variable)]
Reduced renal function (in some patients with structural anomalies) [OMIM:Reduced renal function (in some patients with structural anomalies)]
Quality:
Cross references:
OMIM: "Decreased renal function" [OMIM:Decreased renal function]
OMIM: "Impaired renal function" [OMIM:Impaired renal function]
OMIM: "Renal dysfunction" [OMIM:Renal dysfunction]
OMIM: "Impaired renal function (variable)" [OMIM:Impaired renal function (variable)]
OMIM: "Reduced renal function (in some patients with structural anomalies)" [OMIM:Reduced renal function (in some patients with structural anomalies)]
Is a (Direct Parents):
HPO         Abnormality of the kidney
HPO         Isothenuria
HPO         Abnormality of the urinary system physiology
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)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal physiology(HPO:0012211)
MedDRA:
Database Frequency: 23 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
AA amyloidosis (Orphanet:85445)
Aceruloplasminemia (Orphanet:48818)
Alström syndrome (Orphanet:64)
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 17 (OMIM:615994)
Bardet-Biedl syndrome 6 (OMIM:605231)
Bardet-Biedl syndrome 9 (OMIM:615986)
Bartter syndrome with hypocalcemia (Orphanet:263417)
CORNELIA DE LANGE SYNDROME 1 (OMIM:122470)
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency (Orphanet:93583)
Cushing syndrome (Orphanet:553)
Cystinuria (Orphanet:214)
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome (Orphanet:319678)
Fabry disease (Orphanet:324)
Familial dysautonomia (Orphanet:1764)
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation (Orphanet:324525)
Joubert syndrome 2 (OMIM:608091)
Leigh syndrome (Orphanet:506)
MEDULLARY CYSTIC KIDNEY DISEASE 1 (OMIM:174000)
RENAL DYSPLASIA, CYSTIC, SUSCEPTIBILITY TO (OMIM:601331)
Refsum disease (Orphanet:773)
Thrombotic thrombocytopenic purpura (Orphanet:54057)