Human Phenotype Ontology 
Grandparent Node:
expand
Neoplasm of the endocrine system (HP:0100568)help
Grandparent Node:
expand
Neoplasm of the peripheral nervous system (HP:0100007)help
Parent Node:
expand
Neuroendocrine neoplasm (HP:0100634)help
..Starting node
..expand
Carcinoid tumor (HP:0100570)help
Term ID: 100570
Name: Carcinoid tumor
Synonym: Carcinoid; Carcinoid tumors; Carcinoid tumour; Carcinoid tumours
Definition: A tumor formed from the endocrine (argentaffin) cells of the mucosal lining of a variety of organs including the stomach and intestine. These cells are from neuroectodermal origin.
Comments:
Reference: HP:0100570
Genes and Diseases:
 
       Child Nodes:
........expandSmall intestine carcinoid (HP:0006722) help
........expandIntestinal carcinoid (HP:0006723) help
........expandPulmonary carcinoid tumor (HP:0030445) help
................... HP:0030446 Atypical pulmonary carcinoid tumor

 Sister Nodes: 
..expandPancreatic endocrine tumor (HP:0030405) help
..expandParaganglioma (HP:0002668) help
..expandPheochromocytoma (HP:0002666) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100570HP:0100570Carcinoid tumor0APC CL E G H324583OMIM:175100Adenomatous polyposis coli3179
HP:0100570HP:0100570Carcinoid tumor0APC CL E G H324583ORPHA:79665Gardner syndrome3179
HP:0100570HP:0100570Carcinoid tumor0ATRX CL E G H546886ORPHA:100075Neuroendocrine tumor of stomachHP:0040280 - Obligate169
HP:0100570HP:0100570Carcinoid tumor0CDKN1A CL E G H10261784ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional2
HP:0100570HP:0100570Carcinoid tumor0CDKN1B CL E G H10271785ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional102
HP:0100570HP:0100570Carcinoid tumor0CDKN1B CL E G H10271785ORPHA:276152Multiple endocrine neoplasia type 4HP:0040283 - Occasional102
HP:0100570HP:0100570Carcinoid tumor0CDKN1B CL E G H10271785OMIM:610755Multiple endocrine neoplasia, type IV.102
HP:0100570HP:0100570Carcinoid tumor0CDKN2B CL E G H10301788ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional1
HP:0100570HP:0100570Carcinoid tumor0CDKN2C CL E G H10311789ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional
HP:0100570HP:0100570Carcinoid tumor0DAXX CL E G H16162681ORPHA:100075Neuroendocrine tumor of stomachHP:0040280 - Obligate
HP:0100570HP:0100570Carcinoid tumor0IFNG CL E G H34585438ORPHA:805Tuberous sclerosis complexHP:0040284 - Very rare23
HP:0100570HP:0100570Carcinoid tumor0LMNA CL E G H40006636ORPHA:363618LMNA-related cardiocutaneous progeria syndrome645
HP:0100570HP:0100570Carcinoid tumor0MEN1 CL E G H42217010OMIM:131100Multiple endocrine neoplasia 1462
HP:0100570HP:0100570Carcinoid tumor0MEN1 CL E G H42217010ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional462
HP:0100570HP:0100570Carcinoid tumor0SDHD CL E G H639210683ORPHA:100093Carcinoid syndromeHP:0040280 - Obligate129
HP:0100570HP:0100570Carcinoid tumor0TSC1 CL E G H724812362ORPHA:805Tuberous sclerosis complexHP:0040284 - Very rare1090
HP:0100570HP:0100570Carcinoid tumor0TSC2 CL E G H724912363ORPHA:805Tuberous sclerosis complexHP:0040284 - Very rare2738
HP:0100570HP:0006722Small intestine carcinoid1APC CL E G H324583OMIM:175100Adenomatous polyposis coli.3179
HP:0100570HP:0006722Small intestine carcinoid1APC CL E G H324583ORPHA:79665Gardner syndromeHP:0040284 - Very rare3179
HP:0100570HP:0030445Pulmonary carcinoid tumor1ATRX CL E G H546886ORPHA:100075Neuroendocrine tumor of stomach169
HP:0100570HP:0030445Pulmonary carcinoid tumor1CDKN1A CL E G H10261784ORPHA:652Multiple endocrine neoplasia type 1HP:0040284 - Very rare2
HP:0100570HP:0006723Intestinal carcinoid1CDKN1A CL E G H10261784ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional2
HP:0100570HP:0030445Pulmonary carcinoid tumor1CDKN1B CL E G H10271785ORPHA:652Multiple endocrine neoplasia type 1HP:0040284 - Very rare102
HP:0100570HP:0006723Intestinal carcinoid1CDKN1B CL E G H10271785ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional102
HP:0100570HP:0030445Pulmonary carcinoid tumor1CDKN1B CL E G H10271785ORPHA:276152Multiple endocrine neoplasia type 4HP:0040282 - Frequent102
HP:0100570HP:0006723Intestinal carcinoid1CDKN2B CL E G H10301788ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional1
HP:0100570HP:0030445Pulmonary carcinoid tumor1CDKN2B CL E G H10301788ORPHA:652Multiple endocrine neoplasia type 1HP:0040284 - Very rare1
HP:0100570HP:0006723Intestinal carcinoid1CDKN2C CL E G H10311789ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional
HP:0100570HP:0030445Pulmonary carcinoid tumor1CDKN2C CL E G H10311789ORPHA:652Multiple endocrine neoplasia type 1HP:0040284 - Very rare
HP:0100570HP:0030445Pulmonary carcinoid tumor1DAXX CL E G H16162681ORPHA:100075Neuroendocrine tumor of stomach
HP:0100570HP:0030445Pulmonary carcinoid tumor1LMNA CL E G H40006636ORPHA:363618LMNA-related cardiocutaneous progeria syndromeHP:0040281 - Very frequent645
HP:0100570HP:0030445Pulmonary carcinoid tumor1MEN1 CL E G H42217010ORPHA:652Multiple endocrine neoplasia type 1HP:0040284 - Very rare462
HP:0100570HP:0006723Intestinal carcinoid1MEN1 CL E G H42217010ORPHA:652Multiple endocrine neoplasia type 1HP:0040283 - Occasional462
HP:0100570HP:0030445Pulmonary carcinoid tumor1SDHD CL E G H639210683ORPHA:100093Carcinoid syndromeHP:0040283 - Occasional129
HP:0100570HP:0006722Small intestine carcinoid1SDHD CL E G H639210683ORPHA:100093Carcinoid syndromeHP:0040282 - Frequent129
HP:0100570HP:0006723Intestinal carcinoid1SDHD CL E G H639210683ORPHA:100093Carcinoid syndromeHP:0040282 - Frequent129
HP:0100570HP:0030446Atypical pulmonary carcinoid tumor2ATRX CL E G H546886ORPHA:100075Neuroendocrine tumor of stomachHP:0040283 - Occasional169
HP:0100570HP:0030446Atypical pulmonary carcinoid tumor2DAXX CL E G H16162681ORPHA:100075Neuroendocrine tumor of stomachHP:0040283 - Occasional
HP:0100570HP:0030446Atypical pulmonary carcinoid tumor2SDHD CL E G H639210683ORPHA:100093Carcinoid syndromeHP:0040284 - Very rare129


Genes (13) :APC ATRX CDKN1A CDKN1B CDKN2B CDKN2C DAXX IFNG LMNA MEN1 SDHD TSC1 TSC2

Diseases (10) :OMIM:175100 ORPHA:79665 ORPHA:100075 ORPHA:652 ORPHA:276152 OMIM:610755 ORPHA:805 ORPHA:363618 OMIM:131100 ORPHA:100093
 

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