Absent gallbladder
Symptom Information:
Symptom ID: | HPO:0011467 | |||||
Synonyms: |
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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 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: |
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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) |