Human Phenotype Ontology 
Grandparent Node:
expandAbnormal nervous system morphology (HP:0012639)help
Parent Node:
expandAbnormal peripheral nervous system morphology (HP:0000759)help
..Starting node
..expandNeuritis (HP:0031002)help
Term ID: 31002
Name: Neuritis
Synonym:
Definition: Inflammation of a nerve.
Comments:
Reference: HP:0031002
Genes and Diseases:
 
       Child Nodes:
........expandPolyneuritis (HP:0031003) help

 Sister Nodes: 
..expandAbnormal anterior horn cell morphology (HP:0006802) help
..expandAbnormal cranial nerve morphology (HP:0001291) help
..expandAbnormal lower motor neuron morphology (HP:0002366) help
..expandAbnormal peripheral myelination (HP:0003130) help
..expandAbnormality of peripheral nerves (HP:0045010) help
..expandDecreased size of nerve terminals (HP:0003443) help
..expandDiffuse axonal swelling (HP:0003405) help
..expandEnhanced neurotoxicity of vincristine (HP:0003009) help
..expandHypertrophic nerve changes (HP:0003382) help
..expandMinifascicle formation (HP:0031001) help
..expandNeoplasm of the peripheral nervous system (HP:0100007) help
..expandPeripheral axonal degeneration (HP:0000764) help
..expandPeripheral neuropathy (HP:0009830) 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:0031002HP:0031002Neuritis0 CL E G H
HP:0031002HP:0031003Polyneuritis1 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.