Human Phenotype Ontology 
Grandparent Node:
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Abnormal peripheral nervous system morphology (HP:0000759)help
Grandparent Node:
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Neoplasm of the nervous system (HP:0004375)help
Parent Node:
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Neoplasm of the peripheral nervous system (HP:0100007)help
..Starting node
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Peripheral neuroepithelioma (HP:0006717)help
Term ID: 6717
Name: Peripheral neuroepithelioma
Synonym:
Definition:
Comments:
Reference: HP:0006717
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandNeoplasm of the autonomic nervous system (HP:0030450) help
..expandNeuroendocrine neoplasm (HP:0100634) help
..expandNeurofibromas (HP:0001067) help
..expandNeuroma (HP:0030430) help
..expandSchwannoma (HP:0100008) 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:0006717HP:0006717Peripheral neuroepithelioma0 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 December 15 2022 release.