Human Phenotype Ontology 
Grandparent Node:
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Gait disturbance (HP:0001288)help
Parent Node:
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Unsteady gait (HP:0002317)help
..Starting node
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Gait instability, worse in the dark (HP:0006962)help
Term ID: 6962
Name: Gait instability, worse in the dark
Synonym: Unstable walking, worse in the dark
Definition:
Comments:
Reference: HP:0006962
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006962HP:0006962Gait instability, worse in the dark0RNF170 CL E G H8179025358OMIM:608984Ataxia, sensory, autosomal dominant.3


Genes (1) :RNF170

Diseases (1) :OMIM:608984
 

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