Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal peripheral nervous system morphology (HP:0000759)help
Grandparent Node:
expand
Neoplasm of the nervous system (HP:0004375)help
Parent Node:
expand
Neoplasm of the endocrine system (HP:0100568)help
Parent Node:
expand
Neoplasm of the peripheral nervous system (HP:0100007)help
..Starting node
..expand
Neuroendocrine neoplasm (HP:0100634)help
Term ID: 100634
Name: Neuroendocrine neoplasm
Synonym: Neuroendocrine neoplasia
Definition: A tumor that originates from a neuroendocrine cell.
Comments:
Reference: HP:0100634
Genes and Diseases:
 
       Child Nodes:
........expandPheochromocytoma (HP:0002666) help
................... HP:0006737 Extraadrenal pheochromocytoma
................... HP:0006748 Adrenal pheochromocytoma
........expandParaganglioma (HP:0002668) help
................... HP:0002864 Paraganglioma of head and neck
................... HP:0030074 Chemodectoma
................... HP:0100636 Pulmonary paraglioma
........expandPancreatic endocrine tumor (HP:0030405) help
................... HP:0008261 Pancreatic islet cell adenoma
................... HP:0030404 Glucagonoma
........expandCarcinoid tumor (HP:0100570) help
................... HP:0006722 Small intestine carcinoid
................... HP:0006723 Intestinal carcinoid
................... HP:0030445 Pulmonary carcinoid tumor

 Sister Nodes: 
..expandNeurofibromas (HP:0001067) help
..expandNeuroma (HP:0030430) help
..expandNeuroplasm of the autonomic nervous system (HP:0030450) help
..expandPeripheral neuroepithelioma (HP:0006717) help
..expandSchwannoma (HP:0100008) 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:0100634HP:0100634Neuroendocrine neoplasm0MEN1 CL E G H422197279ORPHA07487010613733
HP:0100634HP:0100634Neuroendocrine neoplasm1MEN1 CL E G H422197279ORPHA07487010613733
HP:0100634HP:0100634Neuroendocrine neoplasm2MEN1 CL E G H422197279ORPHA07487010613733
HP:0100634HP:0100634Neuroendocrine neoplasm3MEN1 CL E G H422197279ORPHA07487010613733


Genes (25) :APC ATRX CDKN1A CDKN1B CDKN2B CDKN2C DAXX FH GCGR KIF1B LMNA MAFA MAX MDH2 MEN1 NF1 PRKAR1A RET SDHA SDHAF2 SDHB SDHC SDHD TMEM127 VHL

Diseases (28) :97279 100075 652 610755 171300 131100 162200 160980 171400 162300 614165 97286 606864 100093 892 193300 79665 175100 276152 29072 438274 363618 1359 601650 115310 605373 168000 147630
 

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