Abnormality of the gallbladder
Symptom Information:
Symptom ID: | HPO:0005264 | |||||||||
Synonyms: |
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Cross references: |
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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) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Hepatobiliary disorders congenital(MedDRA:10019806) Hepatobiliary abnormalities congenital(MedDRA:10019803) Abnormality of the gallbladder(HPO:0005264) |
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Database Frequency: | 14 / 7739 | |||||||||
Resource: |
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) |