Human Phenotype Ontology 
Grandparent Node:
expandAbnormal peripheral nervous system morphology (HP:0000759)help
Parent Node:
expandPeripheral neuropathy (HP:0009830)help
..Starting node
..expandCongenital peripheral neuropathy (HP:0006903)help
Term ID: 6903
Name: Congenital peripheral neuropathy
Synonym:
Definition:
Comments:
Reference: HP:0006903
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAcute episodes of neuropathic symptoms (HP:0003489) help
..expandChronic sensorineural polyneuropathy (HP:0001301) help
..expandDemyelinating peripheral neuropathy (HP:0007108) help
..expandEntrapment neuropathy (HP:0012181) help
..expandEpisodic peripheral neuropathy (HP:0006949) help
..expandMixed demyelinating and axonal polyneuropathy (HP:0007327) help
..expandMononeuropathy (HP:0009831) help
..expandMotor polyneuropathy (HP:0007178) help
..expandPeripheral axonal neuropathy (HP:0003477) help
..expandPolyneuropathy (HP:0001271) help
..expandProgressive peripheral neuropathy (HP:0007133) help
..expandSensorimotor neuropathy (HP:0007141) help
..expandSensorimotor polyneuropathy affecting arms more than legs (HP:0006865) help
..expandSensory neuropathy (HP:0000763) help
..expandSomatic sensory dysfunction (HP:0003474) 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:0006903HP:0006903Congenital peripheral neuropathy0 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.