Recurrent urinary tract infections

Symptom Information:

Symptom ID: HPO:0000010
Synonyms:
Frequent urinary tract infections [HPO:0000010]
Urinary infection [HPO:0000010]
Urinary tract infection [HPO:0000010]
Urinary tract infections [HPO:0000010]
Urinary tract infections, recurrent [HPO:0000010]
Recurrent urinary tract infection [Orphanet:38520]
Recurrent urinary tract infection (disorder) [Orphanet:38520]
Frequent urinary tract infections [OMIM:Frequent urinary tract infections]
Recurrent urinary tract infections [OMIM:Recurrent urinary tract infections]
Urinary infection [OMIM:Urinary infection]
Urinary tract infection [OMIM:Urinary tract infection]
Urinary tract infections [OMIM:Urinary tract infections]
Urinary tract infections, recurrent [OMIM:Urinary tract infections, recurrent]
Recurrent urinary infections [Orphanet:38520]
Recurrent UTI [Orphanet:38520]
Urinary tract infection [MedDRA:10046571]
Chronic UTI [MedDRA:10046571]
Infection urinary tract [MedDRA:10046571]
Lower urinary tract infection [MedDRA:10046571]
Recurrent urinary tract infection [MedDRA:10046571]
Recurrent UTI [MedDRA:10046571]
Urinary infection [MedDRA:10046571]
Urinary tract infection NOS [MedDRA:10046571]
Urinary tract infection, site not specified [MedDRA:10046571]
UTI [MedDRA:10046571]
UTI symptoms [MedDRA:10046571]
Urinary tract infections [MedDRA:10046577]
Quality:
Cross references:
Orphanet:38520 "Recurrent urinary infections" [Orphanet:38520]
OMIM: "Frequent urinary tract infections" [OMIM:Frequent urinary tract infections]
OMIM: "Recurrent urinary tract infections" [OMIM:Recurrent urinary tract infections]
OMIM: "Urinary infection" [OMIM:Urinary infection]
OMIM: "Urinary tract infection" [OMIM:Urinary tract infection]
OMIM: "Urinary tract infections" [OMIM:Urinary tract infections]
OMIM: "Urinary tract infections, recurrent" [OMIM:Urinary tract infections, recurrent]
UMLS:C0262655 "Recurrent urinary tract infection" [Orphanet:38520]
Is a (Direct Parents):
Orphanet Abnormality of the urinary system physiology
HPO         Urinary bladder inflammation
HPO         Recurrent infections
HPO         Recurrent cystitis
HPO         Recurrent pyelonephritis
MedDRA Infections - pathogen unspecified
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 lower urinary tract(HPO:0010936)
                Abnormality of the bladder(HPO:0000014)
                   Urinary bladder inflammation(HPO:0100577)
                      Recurrent urinary tract infections(HPO:0000010)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
             Recurrent infections(HPO:0002719)
                Recurrent urinary tract infections(HPO:0000010)
MedDRA:
Infections and infestations(MedDRA:10021881)
    Infections - pathogen unspecified(MedDRA:10021879)
       Recurrent urinary tract infections(HPO:0000010)
Database Frequency: 56 / 7739
Resource:

All diseases associated with this symptom:

17q12 microdeletion syndrome (Orphanet:261265)
AGAMMAGLOBULINEMIA, X-LINKED (OMIM:300755)
Adenine phosphoribosyltransferase deficiency (Orphanet:976)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Alström syndrome (Orphanet:64)
Autosomal recessive cutis laxa type 1 (Orphanet:90349)
BLADDER DIVERTICULUM (OMIM:109820)
Bardet-Biedl syndrome 10 (OMIM:615987)
Bladder exstrophy (Orphanet:93930)
Cholestasis - pigmentary retinopathy - cleft palate (Orphanet:1415)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Congenital primary megaureter (Orphanet:617)
Currarino triad (Orphanet:1552)
Cutis laxa (Orphanet:209)
Cystinuria (Orphanet:214)
Cystinuria type A (Orphanet:93612)
Cystinuria type B (Orphanet:93613)
Developmental delay-microcephaly-facial dysmorphism syndrome, Hutterite type (Orphanet:363444)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Ehlers-Danlos syndrome type 1 (Orphanet:90309)
Ehlers-Danlos syndrome type 2 (Orphanet:90318)
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis (Orphanet:31043)
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement (Orphanet:2196)
Fanconi anemia (Orphanet:84)
Felty syndrome (Orphanet:47612)
Good syndrome (Orphanet:169105)
Hand-foot-genital syndrome (Orphanet:2438)
Hereditary folate malabsorption (Orphanet:90045)
Hereditary nonpolyposis colon cancer (Orphanet:144)
Hinman syndrome (Orphanet:84085)
Immunodeficiency by defective expression of HLA class 2 (Orphanet:572)
Immunodeficiency with factor I anomaly (Orphanet:200418)
Junctional epidermolysis bullosa (Orphanet:305)
KERATOCONUS POSTICUS CIRCUMSCRIPTUS (OMIM:244600)
Langer-Giedion syndrome (Orphanet:502)
Lymphedema - distichiasis (Orphanet:33001)
Nijmegen breakage syndrome (Orphanet:647)
Occipital horn syndrome (Orphanet:198)
Ochoa syndrome (Orphanet:2704)
Posterior column ataxia - retinitis pigmentosa (Orphanet:88628)
Primary hyperoxaluria type 3 (Orphanet:93600)
Prune belly syndrome (Orphanet:2970)
Purine nucleoside phosphorylase deficiency (Orphanet:760)
Reactive arthritis (Orphanet:29207)
STEVENSON-CAREY SYNDROME (OMIM:611961)
Scalp-ear-nipple syndrome (Orphanet:2036)
Scleroderma (Orphanet:801)
Severe combined immunodeficiency (Orphanet:183660)
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia (Orphanet:632)
Small cell carcinoma of the bladder (Orphanet:284400)
UROFACIAL SYNDROME 1 (OMIM:236730)
UROFACIAL SYNDROME 2 (OMIM:615112)
VESICOURETERAL REFLUX 8 (OMIM:615963)
Williams syndrome (Orphanet:904)
Wolfram syndrome (Orphanet:3463)
Wolfram syndrome 1 (OMIM:222300)