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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Tip-toe gait (HP:0030051)help
Term ID: 30051
Name: Tip-toe gait
Synonym: Walking on tiptoes
Definition: An abnormal gait pattern characterized by the failure of the heel to contact the floor at the onset of stance during gait.
Comments:
Reference: HP:0030051
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
..expandScissor gait (HP:0012407) help
..expandShuffling gait (HP:0002362) help
..expandSteppage gait (HP:0003376) 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:0030051HP:0030051Tip-toe gait0ERLIN1 CL E G H10613401785ORPHA19716947611604
HP:0030051HP:0030051Tip-toe gait0ERLIN1 CL E G H10613615681Spastic paraplegia 62, autosomal recessive615681C4284588OMIM19716947611604
HP:0030051HP:0030051Tip-toe gait0SPG11 CL E G H80208604360Spastic paraplegia 11, autosomal recessive604360C1858479OMIM1216511226610844
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030051HP:0030051Tip-toe gait0DDHD2 CL E G H23259320380ORPHA024929106615003
HP:0030051HP:0030051Tip-toe gait0HARS CL E G H3035488333ORPHA04816142810
HP:0030051HP:0030051Tip-toe gait0KCNA1 CL E G H373637612ORPHA04766218176260
HP:0030051HP:0030051Tip-toe gait0KIF1C CL E G H10749397946ORPHA03666317603060
HP:0030051HP:0030051Tip-toe gait0MT-TE CL E G H45562596HantavirosisORPHA07479590025
HP:0030051HP:0030051Tip-toe gait0SGCG CL E G H6445353Kozlowski Warren Fisher syndromeORPHA048410809608896


Genes (8) :DDHD2 ERLIN1 HARS KCNA1 KIF1C SGCG SPG11 TRNE

Diseases (9) :320380 401785 615681 488333 37612 397946 353 604360 2596
 

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