Human Phenotype Ontology 
Grandparent Node:
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Abnormal nervous system physiology (HP:0012638)help
Parent Node:
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Abnormal central motor function (HP:0011442)help
..Starting node
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Abnormality of central motor conduction (HP:0012079)help
Term ID: 12079
Name: Abnormality of central motor conduction
Synonym:
Definition: Any anomaly of the conduction of motor nerve impulses in the central nervous system.
Comments:
Reference: HP:0012079
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of coordination (HP:0011443) help
..expandAbnormality of extrapyramidal motor function (HP:0002071) help
..expandApraxia (HP:0002186) help
..expandCerebral palsy (HP:0100021) help
..expandobsolete Central hypotonia (HP:0011398) help
..expandParalysis (HP:0003470) help
..expandRigidity (HP:0002063) help
..expandTorticollis (HP:0000473) help
..expandUpper motor neuron dysfunction (HP:0002493) 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:0012079HP:0012079Abnormality of central motor conduction0POLG CL E G H54289179ORPHA:94125Recessive mitochondrial ataxia syndromeHP:0040282 - Frequent464
HP:0012079HP:0034399Prolonged central motor conduction time1 CL E G H


Genes (1) :POLG

Diseases (1) :ORPHA:94125
 

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