Recurrent urinary tract infections
Symptom Information:
Symptom ID: | HPO:0000010 | |||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): | ||||||||||||||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the immune system(HPO:0002715) Abnormality of immune system physiology(HPO:0010978) Recurrent infections(HPO:0002719) Recurrent urinary tract infections(HPO:0000010) 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) MedDRA: Infections and infestations(MedDRA:10021881) Infections - pathogen unspecified(MedDRA:10021879) Recurrent urinary tract infections(HPO:0000010) |
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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) |