Absent gallbladder

Symptom Information:

Symptom ID: HPO:0011467
Synonyms:
Agenesis of the gallbladder [HPO:0011467]
Aplasia of the gallbladder [HPO:0011467]
Absent gallbladder [OMIM:Absent gallbladder]
Agenesis of the gallbladder [OMIM:Agenesis of the gallbladder]
Absent gallbladder (male) [OMIM:Absent gallbladder (male)]
Quality:
Cross references:
OMIM: "Absent gallbladder" [OMIM:Absent gallbladder]
OMIM: "Agenesis of the gallbladder" [OMIM:Agenesis of the gallbladder]
OMIM: "Absent gallbladder (male)" [OMIM:Absent gallbladder (male)]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the gallbladder
Is a (Whole tree): HPO:
All(HPO:0000001)
    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)
                      Abnormal gallbladder morphology(HPO:0012437)
                         Aplasia/Hypoplasia of the gallbladder(HPO:0011466)
                            Absent gallbladder(HPO:0011467)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
Holoprosencephaly - radial heart renal anomalies (Orphanet:3186)
Intellectual deficit, X-linked - craniofacioskeletal syndrome (Orphanet:163979)
MITCHELL-RILEY SYNDROME (OMIM:615710)
Microgastria - limb reduction defect (Orphanet:2538)
Opitz G/BBB syndrome (Orphanet:2745)