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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Scissor gait (HP:0012407)help
Term ID: 12407
Name: Scissor gait
Synonym: Scissor gait; Scissor walk; Scissors gait
Definition: A type of spastic paraparetic gait in which the muscle tone in the adductors is marked. It is characterized by hypertonia and flexion in the legs, hips and pelvis accompanied by extreme adduction leading to the knees and thighs hitting, or sometimes even crossing, in a scissors-like movement. The opposing muscles (abductors) become comparatively weak from lack of use.
Comments:
Reference: HP:0012407
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
..expandImpaired tandem gait (HP:0031629) help
..expandInability to walk (HP:0002540) 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:0012407HP:0012407Scissor gait0AMPD2 CL E G H271401805ORPHA1230469102771
HP:0012407HP:0012407Scissor gait0AMPD2 CL E G H271401805ORPHA1172469102771
HP:0012407HP:0012407Scissor gait0AMPD2 CL E G H271615686Spastic paraplegia 63, autosomal recessive615686C3810295OMIM1230469102771
HP:0012407HP:0012407Scissor gait0AMPD2 CL E G H271615686Spastic paraplegia 63, autosomal recessive615686C3810295OMIM1172469102771
HP:0012407HP:0012407Scissor gait0ARL6IP1 CL E G H23204401780ORPHA159697607669
HP:0012407HP:0012407Scissor gait0ARL6IP1 CL E G H23204401780ORPHA158697607669
HP:0012407HP:0012407Scissor gait0ARL6IP1 CL E G H23204615685Spastic paraplegia 61, autosomal recessive615685C3810294OMIM159697607669
HP:0012407HP:0012407Scissor gait0ARL6IP1 CL E G H23204615685Spastic paraplegia 61, autosomal recessive615685C3810294OMIM158697607669
HP:0012407HP:0012407Scissor gait0FBXO7 CL E G H25793260300Parkinson disease 15260300C1850100OMIM118313586605648
HP:0012407HP:0012407Scissor gait0FBXO7 CL E G H25793260300Parkinson disease 15260300C1850100OMIM116113586605648
HP:0012407HP:0012407Scissor gait0KIF1A CL E G H547101010ORPHA11735888601255
HP:0012407HP:0012407Scissor gait0KIF1A CL E G H547101010ORPHA11441888601255
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012407HP:0012407Scissor gait0ATP6AP2 CL E G H10159363654ORPHA028618305300556
HP:0012407HP:0012407Scissor gait0ATP6AP2 CL E G H10159363654ORPHA026318305300556


Genes (5) :AMPD2 ARL6IP1 ATP6AP2 FBXO7 KIF1A

Diseases (7) :401805 615686 401780 615685 363654 260300 101010
 

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