Human Phenotype Ontology 
Grandparent Node:
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Neoplasm of the peripheral nervous system (HP:0100007)help
Parent Node:
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Abnormality of the vestibulocochlear nerve (HP:0009591)help
Parent Node:
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Neoplasm of the inner ear (HP:0040096)help
Parent Node:
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Schwannoma (HP:0100008)help
..Starting node
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Vestibular schwannoma (HP:0009588)help
Term ID: 9588
Name: Vestibular schwannoma
Synonym: Acoustic Neuroma; Vestibular neurilemmoma; Vestibular neurinoma; Vestibular neurolemmoma; Vestibular Schwann cell tumor; Vestibular Schwann cell tumour
Definition: A vestibular schwannoma (also known as acoustic neuroma, acoustic neurinoma, or acoustic neurilemoma) is a benign, usually slow-growing tumor that develops from the VIIIth cranial nerve supplying the inner ear.
Comments:
Reference: HP:0009588
Genes and Diseases:
 
       Child Nodes:
........expandBilateral vestibular Schwannoma (HP:0009589) help
........expandUnilateral vestibular Schwannoma (HP:0009590) help

 Sister Nodes: 
..expandPeripheral Schwannoma (HP:0009593) help
..expandScleral schwannoma (HP:0100011) 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:0009588HP:0009588Vestibular schwannoma0HRAS CL E G H32655173OMIM:218040Costello syndrome.113
HP:0009588HP:0009588Vestibular schwannoma0KARS1 CL E G H37356215OMIM:613641Charcot-marie-tooth disease, recessive intermediate B.
HP:0009588HP:0009588Vestibular schwannoma0NF2 CL E G H47717773ORPHA:637Neurofibromatosis type 2220
HP:0009588HP:0009588Vestibular schwannoma0NF2 CL E G H47717773OMIM:101000Neurofibromatosis, type II220
HP:0009588HP:0009588Vestibular schwannoma0SPRED1 CL E G H16174220249ORPHA:137605Legius syndrome136
HP:0009588HP:0009589Bilateral vestibular schwannoma1NF2 CL E G H47717773ORPHA:637Neurofibromatosis type 2HP:0040282 - Frequent220
HP:0009588HP:0009590Unilateral vestibular schwannoma1NF2 CL E G H47717773OMIM:101000Neurofibromatosis, type II220
HP:0009588HP:0009589Bilateral vestibular schwannoma1NF2 CL E G H47717773OMIM:101000Neurofibromatosis, type II220


Genes (4) :HRAS KARS1 NF2 SPRED1

Diseases (5) :OMIM:218040 OMIM:613641 ORPHA:637 OMIM:101000 ORPHA:137605
 

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