Bladder diverticulum
Symptom Information:
Symptom ID: | HPO:0000015 | ||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) Bladder diverticulum(HPO:0000015) MedDRA: Renal and urinary disorders(MedDRA:10038359) Bladder and bladder neck disorders (excl calculi)(MedDRA:10004994) Bladder disorders NEC(MedDRA:10005037) Bladder diverticulum(HPO:0000015) |
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Database Frequency: | 15 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Autosomal recessive cutis laxa type 1 | (Orphanet:90349) |
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA | (OMIM:219100) |
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies | (Orphanet:221145) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 | (OMIM:129900) |
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 | (OMIM:604292) |
EEC syndrome | (Orphanet:1896) |
Ehlers-Danlos syndrome type 1 | (Orphanet:90309) |
Ehlers-Danlos syndrome type 2 | (Orphanet:90318) |
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type | (Orphanet:300179) |
Ehlers-Danlos syndrome, kyphoscoliotic type | (Orphanet:1900) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Marfanoid syndrome, De Silva type | (Orphanet:2464) |
Menkes disease | (Orphanet:565) |
Occipital horn syndrome | (Orphanet:198) |
Williams syndrome | (Orphanet:904) |