Human Phenotype Ontology 
Grandparent Node:
Abnormality of the gastrointestinal tract (HP:0011024)help
Grandparent Node:
Neoplasm by anatomical site (HP:0011793)help
Parent Node:
Carcinoid tumor (HP:0100570)help
Parent Node:
Neoplasm of the gastrointestinal tract (HP:0007378)help
..Starting node
Intestinal carcinoid (HP:0006723)help
Term ID: 6723
Name: Intestinal carcinoid
Reference: HP:0006723
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 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
..expandPrimary peritoneal carcinoma (HP:0030406) help
..expandZollinger-Ellison syndrome (HP:0002044) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HP:0006723HP:0006723Intestinal carcinoid0SDHD CL E G H6392100093ORPHA150710683602690
HP:0006723HP:0006723Intestinal carcinoid0SDHD CL E G H6392100093ORPHA144210683602690
HPO disease - gene - phenotype less frequent non-typical associations:

Genes (1) :SDHD

Diseases (1) :100093

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.