Human Phenotype Ontology 
Grandparent Node:
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Abnormal biliary tract morphology (HP:0012440)help
Grandparent Node:
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Neoplasm of the gastrointestinal tract (HP:0007378)help
Parent Node:
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Abnormal gallbladder morphology (HP:0012437)help
Parent Node:
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Biliary tract neoplasm (HP:0100574)help
..Starting node
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Neoplasm of the gallbladder (HP:0100575)help
Term ID: 100575
Name: Neoplasm of the gallbladder
Synonym: Neoplasia of the gallbladder
Definition: The presence of a neoplasm of the gallbladder.
Comments:
Reference: HP:0100575
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCholangiocarcinoma (HP:0030153) help
..expandMultiple biliary hamartomas (HP:0025519) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100575HP:0100575Neoplasm of the gallbladder0ARSA CL E G H410713ORPHA:309271Metachromatic leukodystrophy, adult formHP:0040284 - Very rare253
HP:0100575HP:0100575Neoplasm of the gallbladder0GPR35 CL E G H28594492ORPHA:171Primary sclerosing cholangitisHP:0040284 - Very rare2
HP:0100575HP:0100575Neoplasm of the gallbladder0MST1 CL E G H44857380ORPHA:171Primary sclerosing cholangitisHP:0040284 - Very rare1
HP:0100575HP:0100575Neoplasm of the gallbladder0PSAP CL E G H56609498ORPHA:309271Metachromatic leukodystrophy, adult formHP:0040284 - Very rare81
HP:0100575HP:0100575Neoplasm of the gallbladder0SEMA4D CL E G H1050710732ORPHA:171Primary sclerosing cholangitisHP:0040284 - Very rare
HP:0100575HP:0100575Neoplasm of the gallbladder0TCF4 CL E G H692511634ORPHA:171Primary sclerosing cholangitisHP:0040284 - Very rare241


Genes (6) :ARSA GPR35 MST1 PSAP SEMA4D TCF4

Diseases (2) :ORPHA:309271 ORPHA:171
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.