Abnormality of the gallbladder

Symptom Information:

Symptom ID: HPO:0005264
Gallbladder anomaly [Orphanet:28110]
Congenital anomaly of gallbladder (disorder) [Orphanet:28110]
Gallbladder anomalies (disorder) [Orphanet:28110]
Gallbladder anomaly congenital [Orphanet:28110]
Gallbladder/common bile duct anomalies [Orphanet:28110]
Gallbladder anomaly congenital [MedDRA:10061163]
Congenital abnormal forms gallbladder [MedDRA:10061163]
Gallbladder anomaly congenital NOS [MedDRA:10061163]
Common bile duct anomaly [Orphanet:28110]
Cross references:
Orphanet:28110 "Gallbladder/common bile duct anomalies" [Orphanet:28110]
UMLS:C0266249 "Gallbladder anomaly congenital" [Orphanet:28110]
Is a (Direct Parents):
MedDRA Hepatobiliary abnormalities congenital
HPO         Abnormality of the biliary system
Orphanet Biliary tract abnormality
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the liver(HPO:0001392)
                Abnormality of the biliary system(HPO:0004297)
                   Abnormality of the gallbladder(HPO:0005264)
Congenital, familial and genetic disorders(MedDRA:10010331)
    Hepatobiliary disorders congenital(MedDRA:10019806)
       Hepatobiliary abnormalities congenital(MedDRA:10019803)
          Abnormality of the gallbladder(HPO:0005264)
Database Frequency: 14 / 7739

All diseases associated with this symptom:

Acrocephalosyndactyly (Orphanet:946)
Cantrell pentalogy (Orphanet:1335)
Congenital alveolar capillary dysplasia (Orphanet:210122)
Congenital bile acid synthesis defect type 4 (Orphanet:79095)
Craniomicromelic syndrome (Orphanet:1524)
Fucosidosis (Orphanet:349)
Genito-palato-cardiac syndrome (Orphanet:2075)
Hashimoto-Pritzker syndrome (Orphanet:99872)
Holoprosencephaly - radial heart renal anomalies (Orphanet:3186)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Triploidy (Orphanet:3376)
VACTERL/VATER association (Orphanet:887)
Wilson disease (Orphanet:905)
Wolf-Hirschhorn syndrome (Orphanet:280)