Human Phenotype Ontology 
Grandparent Node:
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Abnormal nervous system physiology (HP:0012638)help
Parent Node:
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Abnormality of higher mental function (HP:0011446)help
..Starting node
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Optic ataxia (HP:0031868)help
Term ID: 31868
Name: Optic ataxia
Synonym:
Definition: Difficulty reaching to visually guided goals in peripheral vision, with the deficit leaves voluntary eye movements largely unaffected.
Comments:
Reference: HP:0031868
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAgnosia (HP:0010524) help
..expandApraxia (HP:0002186) help
..expandCognitive impairment (HP:0100543) help
..expandLanguage impairment (HP:0002463) help
..expandMicrographia (HP:0031908) help
..expandNeurological speech impairment (HP:0002167) help
..expandReduced consciousness/confusion (HP:0004372) 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:0031868HP:0031868Optic ataxia0APOE CL E G H348613OMIM:607822Alzheimer disease 3.39
HP:0031868HP:0031868Optic ataxia0PSEN1 CL E G H56639508OMIM:607822Alzheimer disease 3.241


Genes (2) :APOE PSEN1

Diseases (1) :OMIM:607822
 

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