Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormality of the gallbladder (HP:0005264)

Parent Node:
Abnormal gallbladder morphology (HP:0012437)

..Starting node
..Gallbladder perforation (HP:0030154)

Term ID:

30154

Name:

Gallbladder perforation

Synonym:

Gall bladder perforation

Definition:

Rupture of the wall of the gallbladder.

Comments:

Reference:

HP:0030154

Genes and Diseases:

Child Nodes:

Sister Nodes:

Aplasia/Hypoplasia of the gallbladder (HP:0011466)

Bilobate gallbladder (HP:0005608)

Cholelithiasis (HP:0001081)

Cystic artery pseudoaneurysm (HP:0030170)

Neoplasm of the gallbladder (HP:0100575)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030154	HP:0030154	Gallbladder perforation	0	CL E G H

Genes (0) :

Diseases (0) :

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