Abnormality of renal resorption

Symptom Information:

Symptom ID: HPO:0011038
Synonyms:
Renal tubular disease [Orphanet:38120]
Renal tubular defect (disorder) [Orphanet:38120]
Renal tubular disorder (disorder) [Orphanet:38120]
Renal tubular disorder [Orphanet:38120]
Renal tubular defect [Orphanet:38120]
Renal tubular defect/tubulopathy [Orphanet:38120]
Renal tubular disorder [MedDRA:10038537]
Disorder tubular kidney [MedDRA:10038537]
Distal renal tubular dysfunction [MedDRA:10038537]
Kidney tubular disorder [MedDRA:10038537]
Kidney tubule disorder [MedDRA:10038537]
Nephropathy tubular [MedDRA:10038537]
Proximal renal tubular dysfunction [MedDRA:10038537]
Renal tubular disorder acute [MedDRA:10038537]
Renal tubular disorder NOS [MedDRA:10038537]
Renal tubular dysfunction [MedDRA:10038537]
Quality:
Cross references:
HPO:0000124 "Renal tubular dysfunction" [Orphanet:38120]
Orphanet:38120 "Renal tubular defect/tubulopathy" [Orphanet:38120]
UMLS:C0151747 "Renal tubular disorder" [Orphanet:38120]
UMLS:C0268709 "Renal tubular defect" [Orphanet:38120]
Is a (Direct Parents):
Orphanet Nephropathy
HPO         Abnormal renal physiology
MedDRA Nephropathies and tubular disorders NEC
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 renal resorption(HPO:0011038)
             Abnormality of the upper urinary tract(HPO:0010935)
                Abnormality of the kidney(HPO:0000077)
                   Abnormal renal physiology(HPO:0012211)
                      Abnormality of renal resorption(HPO:0011038)
MedDRA:
Renal and urinary disorders(MedDRA:10038359)
    Nephropathy(HPO:0000112)
       Nephropathies and tubular disorders NEC(MedDRA:10029150)
          Abnormality of renal resorption(HPO:0011038)
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
Cystinosis (Orphanet:213)
Fanconi renotubular syndrome 1 (OMIM:134600)
Glycogen storage disease due to GLUT2 deficiency (Orphanet:2088)
MELAS (Orphanet:550)
Wilson disease (Orphanet:905)