Bladder exstrophy

Symptom Information:

Symptom ID: HPO:0002836
Synonyms:
Exstrophy (morphologic abnormality) [Orphanet:37520]
Exstrophy of bladder sequence (disorder) [Orphanet:37520]
Bladder Exstrophy [Orphanet:37520]
Exstrophy [Orphanet:37520]
Bladder exstrophy [OMIM:Bladder exstrophy]
Bladder/cloacal exstrophy [Orphanet:37520]
Bladder exstrophy (in 1 of 6 patients) [OMIM:Bladder exstrophy (in 1 of 6 patients)]
Quality:
Cross references:
HPO:0100548 "Exstrophy" [Orphanet:37520]
Orphanet:37520 "Bladder/cloacal exstrophy" [Orphanet:37520]
OMIM: "Bladder exstrophy" [OMIM:Bladder exstrophy]
OMIM: "Bladder exstrophy (in 1 of 6 patients)" [OMIM:Bladder exstrophy (in 1 of 6 patients)]
UMLS:C0005689 "Bladder Exstrophy" [Orphanet:37520]
UMLS:C0015338 "Exstrophy" [Orphanet:37520]
Is a (Direct Parents):
HPO         Abnormality of the bladder
HPO         Exstrophy
Orphanet Bladder and ureter anomalies
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 exstrophy(HPO:0002836)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal wall(HPO:0004298)
             Exstrophy(HPO:0100548)
                Bladder exstrophy(HPO:0002836)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Beta-ureidopropionase deficiency (Orphanet:65287)
Bladder exstrophy (Orphanet:93930)
Constriction rings syndrome (Orphanet:295000)
Diabetic embryopathy (Orphanet:1926)
Exstrophy-epispadias complex (Orphanet:322)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III (OMIM:210730)
Terminal transverse defects of arm (Orphanet:93937)
Toriello-Lacassie-Droste syndrome (Orphanet:3339)