Human Phenotype Ontology 
Grandparent Node:
Abnormality of the endocrine system (HP:0000818)help
Grandparent Node:
Neoplasm by anatomical site (HP:0011793)help
Parent Node:
Neoplasm of the endocrine system (HP:0100568)help
..Starting node
APUdoma (HP:0040192)help
Term ID: 40192
Name: APUdoma
Synonym: amine precursor uptake and decarboxylation tumours
Definition: An endocrine tumor arising from an APUD cell.
Reference: HP:0040192
Genes and Diseases:
       Child Nodes:
........expandMerkel cell skin cancer (HP:0030447) help

 Sister Nodes: 
..expandNeoplasm of the adrenal gland (HP:0100631) help
..expandNeoplasm of the parathyroid gland (HP:0100733) help
..expandNeoplasm of the pituitary gland (HP:0040277) help
..expandNeoplasm of the thyroid gland (HP:0100031) help
..expandNeuroendocrine neoplasm (HP:0100634) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040192HP:0040192APUdoma0 CL E G H
HP:0040192HP:0040192APUdoma1 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 June 2019 release.