Pyelonephritis

Symptom Information:

Symptom ID: HPO:0012330
Synonyms:
Pyelonephritis [OMIM:Pyelonephritis]
Pyelonephritis (in some patients) [OMIM:Pyelonephritis (in some patients)]
Pyelonephritis [MedDRA:10037596]
Quality:
Cross references:
OMIM: "Pyelonephritis" [OMIM:Pyelonephritis]
OMIM: "Pyelonephritis (in some patients)" [OMIM:Pyelonephritis (in some patients)]
Is a (Direct Parents):
HPO         Recurrent pyelonephritis
HPO         Nephritis
MedDRA Recurrent urinary tract infections
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)
                      Nephritis(HPO:0000123)
                         Pyelonephritis(HPO:0012330)
             Abnormality of the urinary system physiology(HPO:0011277)
                Abnormal renal physiology(HPO:0012211)
                   Nephritis(HPO:0000123)
                      Pyelonephritis(HPO:0012330)
MedDRA:
Infections and infestations(MedDRA:10021881)
    Infections - pathogen unspecified(MedDRA:10021879)
       Recurrent urinary tract infections(HPO:0000010)
          Pyelonephritis(HPO:0012330)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
Hereditary xanthinuria (Orphanet:3467)
Immunodeficiency with factor I anomaly (Orphanet:200418)
Isobutyryl-CoA dehydrogenase deficiency (Orphanet:79159)
Rabson-Mendenhall syndrome (Orphanet:769)
Scalp-ear-nipple syndrome (Orphanet:2036)
Xanthinuria type I (Orphanet:93601)