Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the gastrointestinal tract (HP:0011024)help
Grandparent Node:
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Neoplasm by anatomical site (HP:0011793)help
Parent Node:
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Neoplasm of the gastrointestinal tract (HP:0007378)help
..Starting node
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Primary peritoneal carcinoma (HP:0030406)help
Term ID: 30406
Name: Primary peritoneal carcinoma
Synonym:
Definition: A type of cancer that originates in the peritoneam. It is to be distinguished from metastatic cancer of the peritoneum. Peritoneal cancer can occur anywhere in the abdominal space, and affects the surface of organs contained inside the peritoneum.
Comments:
Reference: HP:0030406
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAmpulla of Vater carcinoma (HP:0031524) help
..expandBenign gastrointestinal tract tumors (HP:0006719) help
..expandBiliary tract neoplasm (HP:0100574) help
..expandDesmoid tumors (HP:0100245) help
..expandEsophageal neoplasm (HP:0100751) help
..expandGastrointestinal stroma tumor (HP:0100723) help
..expandIntestinal carcinoid (HP:0006723) help
..expandIntestinal polyp (HP:0005266) help
..expandMalignant gastrointestinal tract tumors (HP:0006749) help
..expandMultiple intestinal neurofibromatosis (HP:0005220) help
..expandNeoplasm of the large intestine (HP:0100834) help
..expandNeoplasm of the liver (HP:0002896) help
..expandNeoplasm of the small intestine (HP:0100833) help
..expandNeoplasm of the stomach (HP:0006753) help
..expandZollinger-Ellison syndrome (HP:0002044) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0030406HP:0030406Primary peritoneal carcinoma0BARD1 CL E G H580145Hereditary breast and ovarian cancer syndromeC0677776ORPHA1125952601593
HP:0030406HP:0030406Primary peritoneal carcinoma0BRCA1 CL E G H672145Hereditary breast and ovarian cancer syndromeC0677776ORPHA128241100113705
HP:0030406HP:0030406Primary peritoneal carcinoma0BRCA2 CL E G H675145Hereditary breast and ovarian cancer syndromeC0677776ORPHA130251101600185
HP:0030406HP:0030406Primary peritoneal carcinoma0BRIP1 CL E G H83990145Hereditary breast and ovarian cancer syndromeC0677776ORPHA120220473605882
HP:0030406HP:0030406Primary peritoneal carcinoma0CHEK2 CL E G H11200145Hereditary breast and ovarian cancer syndromeC0677776ORPHA121316627604373
HP:0030406HP:0030406Primary peritoneal carcinoma0MRE11 CL E G H4361145Hereditary breast and ovarian cancer syndromeC0677776ORPHA1577230600814
HP:0030406HP:0030406Primary peritoneal carcinoma0NBN CL E G H4683145Hereditary breast and ovarian cancer syndromeC0677776ORPHA11487652602667
HP:0030406HP:0030406Primary peritoneal carcinoma0PALB2 CL E G H79728145Hereditary breast and ovarian cancer syndromeC0677776ORPHA141726144610355
HP:0030406HP:0030406Primary peritoneal carcinoma0PTEN CL E G H5728145Hereditary breast and ovarian cancer syndromeC0677776ORPHA16589588601728
HP:0030406HP:0030406Primary peritoneal carcinoma0RAD50 CL E G H10111145Hereditary breast and ovarian cancer syndromeC0677776ORPHA1959816604040
HP:0030406HP:0030406Primary peritoneal carcinoma0RAD51 CL E G H5888145Hereditary breast and ovarian cancer syndromeC0677776ORPHA1169817179617
HP:0030406HP:0030406Primary peritoneal carcinoma0RAD51C CL E G H5889145Hereditary breast and ovarian cancer syndromeC0677776ORPHA11319820602774
HP:0030406HP:0030406Primary peritoneal carcinoma0RAD51D CL E G H5892145Hereditary breast and ovarian cancer syndromeC0677776ORPHA1869823602954
HP:0030406HP:0030406Primary peritoneal carcinoma0TP53 CL E G H7157145Hereditary breast and ovarian cancer syndromeC0677776ORPHA154111998191170
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (14) :BARD1 BRCA1 BRCA2 BRIP1 CHEK2 MRE11 NBN PALB2 PTEN RAD50 RAD51 RAD51C RAD51D TP53

Diseases (1) :145
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.