Human Phenotype Ontology 
Grandparent Node:
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Abnormality of nervous system morphology (HP:0012639)help
Grandparent Node:
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Neoplasm by anatomical site (HP:0011793)help
Parent Node:
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Abnormal peripheral nervous system morphology (HP:0000759)help
Parent Node:
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Neoplasm of the nervous system (HP:0004375)help
..Starting node
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Neoplasm of the peripheral nervous system (HP:0100007)help
Term ID: 100007
Name: Neoplasm of the peripheral nervous system
Synonym: Tumor of the peripheral nervous system
Definition: A benign or malignant neoplasm (tumour) of the peripheral nervous system.
Comments:
Reference: HP:0100007
Genes and Diseases:
 
       Child Nodes:
........expandNeurofibromas (HP:0001067) help
................... HP:0005220 Multiple intestinal neurofibromatosis
................... HP:0006751 Paraspinal neurofibromas
................... HP:0007524 Atypical neurofibromatosis
................... HP:0007576 Palmar neurofibromas
................... HP:0009595 Occasional neurofibromas
................... HP:0009732 Plexiform neurofibroma
................... HP:0009735 Spinal neurofibromas
................... HP:0100698 Subcutaneous neurofibromas
........expandPeripheral neuroepithelioma (HP:0006717) help
........expandNeuroma (HP:0030430) help
................... HP:0031023 Multiple mucosal neuromas
........expandNeuroplasm of the autonomic nervous system (HP:0030450) help
................... HP:0003005 Ganglioneuroma
........expandSchwannoma (HP:0100008) help
................... HP:0009588 Vestibular Schwannoma
................... HP:0009593 Peripheral Schwannoma
................... HP:0100011 Scleral schwannoma
........expandNeuroendocrine neoplasm (HP:0100634) help
................... HP:0002666 Pheochromocytoma
................... HP:0002668 Paraganglioma
................... HP:0030405 Pancreatic endocrine tumor
................... HP:0100570 Carcinoid tumor

 Sister Nodes: 
..expandNeoplasm of the central nervous system (HP:0100006) 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:0100007HP:0100007Neoplasm of the peripheral nervous system0 CL E G H
HP:0100007HP:0100007Neoplasm of the peripheral nervous system1 CL E G H
HP:0100007HP:0100007Neoplasm of the peripheral nervous system2 CL E G H
HP:0100007HP:0100007Neoplasm of the peripheral nervous system3 CL E G H
HP:0100007HP:0100007Neoplasm of the peripheral nervous system4 CL E G H


Genes (42) :APC ASCL1 ATRX BDNF CCM2 CDKN1A CDKN1B CDKN2B CDKN2C DAXX EDN3 FH GCGR GDNF HRAS KARS KIF1B KIT KRIT1 LMNA MAFA MAX MDH2 MEN1 MYO1H NF1 NF2 NME1 PDCD10 PDGFRA PHOX2B PRKAR1A RET RNF43 SDHA SDHAF2 SDHB SDHC SDHD SPRED1 TMEM127 VHL

Diseases (45) :221061 606764 97279 193520 162091 160980 157798 611431 209880 99803 100075 661 652 610755 218040 613641 171300 131100 162200 601321 637 101000 256700 613013 1359 171400 162300 614165 97286 606864 100093 892 193300 79665 175100 276152 29072 438274 363618 162210 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.