Human Phenotype Ontology 
Grandparent Node:
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Abnormality of movement (HP:0100022)help
Parent Node:
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Gait disturbance (HP:0001288)help
..Starting node
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Impaired tandem gait (HP:0031629)help
Term ID: 31629
Name: Impaired tandem gait
Synonym: Clumsy tandem walking
Definition: Reduced ability to walk in a straight line while placing the feet heel to toe.
Comments:
Reference: HP:0031629
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBroad-based gait (HP:0002136) help
..expandCerebellar ataxia associated with quadrupedal gait (HP:0009878) help
..expandCock-walk gait (HP:0031848) help
..expandDifficulty walking (HP:0002355) help
..expandDifficulty walking backward (HP:0031847) help
..expandFalls (HP:0002527) help
..expandFreezing of gait (HP:0031825) help
..expandGait apraxia (HP:0010521) help
..expandGait ataxia (HP:0002066) help
..expandGait imbalance (HP:0002141) help
..expandHobby horse gait (HP:0031856) help
..expandInability to walk (HP:0002540) help
..expandScissor gait (HP:0012407) help
..expandShuffling gait (HP:0002362) help
..expandSteppage gait (HP:0003376) help
..expandTip-toe gait (HP:0030051) help
..expandToe walking (HP:0040083) help
..expandUnsteady gait (HP:0002317) help
..expandWaddling gait (HP:0002515) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0031629HP:0031629Impaired tandem gait0FMR1 CL E G H2332300623Fragile X tremor/ataxia syndrome300623C1839780OMIM13223775309550
HP:0031629HP:0031629Impaired tandem gait0FMR1 CL E G H2332300623Fragile X tremor/ataxia syndrome300623C1839780OMIM13173775309550
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :FMR1

Diseases (1) :300623
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.