Bladder diverticulum

Symptom Information:

Symptom ID: HPO:0000015
Synonyms:
Diverticulum of bladder (disorder) [Orphanet:37560]
Diverticulum of bladder [Orphanet:37560]
Bladder/vesical diverticulum [Orphanet:37560]
Bladder diverticulum [Orphanet:37560]
Bladder diverticulum [MedDRA:10005038]
Diverticulum of bladder [MedDRA:10005038]
Bladder diverticula [OMIM:Bladder diverticula]
Bladder diverticulum (in some patients) [OMIM:Bladder diverticulum (in some patients)]
Quality:
Cross references:
Orphanet:37560 "Bladder/vesical diverticulum" [Orphanet:37560]
OMIM: "Bladder diverticula" [OMIM:Bladder diverticula]
OMIM: "Bladder diverticulum (in some patients)" [OMIM:Bladder diverticulum (in some patients)]
UMLS:C0156273 "Diverticulum of bladder" [Orphanet:37560]
Is a (Direct Parents):
Orphanet Bladder and ureter anomalies
HPO         Abnormality of the bladder
MedDRA Bladder 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 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)
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)