| 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: |
.. Broad-based gait (HP:0002136) 
|
..Cerebellar ataxia associated with quadrupedal gait (HP:0009878)
|
..Cock-walk gait (HP:0031848)
|
..Difficulty walking (HP:0002355)
|
..Difficulty walking backward (HP:0031847)
|
..Falls (HP:0002527)
|
..Freezing of gait (HP:0031825)
|
..Gait apraxia (HP:0010521)
|
..Gait ataxia (HP:0002066)
|
..Gait imbalance (HP:0002141)
|
..Hobby horse gait (HP:0031856)
|
..Inability to walk (HP:0002540)
|
..obsolete Toe walking (HP:0040083)
|
..Scissor gait (HP:0012407)
|
..Shuffling gait (HP:0002362)
|
..Steppage gait (HP:0003376)
|
..Tip-toe gait (HP:0030051)
|
..Unsteady gait (HP:0002317)
|
..Waddling gait (HP:0002515)
|
| Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
|---|
HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: | | HP:0031629 | HP:0031629 | Impaired tandem gait | 0 | ATP6AP2 CL E G H | 10159 | 18305 | OMIM:300423 | MENTAL RETARDATION, X-LINKED, SYNDROMIC, HEDERA TYPE; MRXSH | | | | 36 | | | | HP:0031629 | HP:0031629 | Impaired tandem gait | 0 | COQ5 CL E G H | 84274 | 28722 | OMIM:619028 | COENZYME Q10 DEFICIENCY, PRIMARY, 9; COQ10D9 | | | | | | | | HP:0031629 | HP:0031629 | Impaired tandem gait | 0 | FMR1 CL E G H | 2332 | 3775 | OMIM:300623 | Fragile X tremor/ataxia syndrome | . | | | 30 | | | | HP:0031629 | HP:0031629 | Impaired tandem gait | 0 | GDAP1 CL E G H | 54332 | 15968 | ORPHA:101097 | Autosomal recessive Charcot-Marie-Tooth disease with hoarseness | | | | 108 | | | | HP:0031629 | HP:0031629 | Impaired tandem gait | 0 | ITPR1 CL E G H | 3708 | 6180 | OMIM:117360 | Spinocerebellar ataxia 29 | | | | 177 | | | | HP:0031629 | HP:0031629 | Impaired tandem gait | 0 | JAG1 CL E G H | 182 | 6188 | OMIM:619574 | CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2HH; CMT2HH | | | | 257 | | | | HP:0031629 | HP:0031629 | Impaired tandem gait | 0 | KCNN2 CL E G H | 3781 | 6291 | OMIM:619724 | DYSTONIA 34, MYOCLONIC; DYT34 | | | | | | | | HP:0031629 | HP:0031629 | Impaired tandem gait | 0 | MTRFR CL E G H | 91574 | 26784 | ORPHA:254930 | Combined oxidative phosphorylation defect type 7 | HP:0040282 - Frequent | | | | | | | HP:0031629 | HP:0031629 | Impaired tandem gait | 0 | PCDH15 CL E G H | 65217 | 14674 | OMIM:602083 | Usher syndrome, type IF | | | | 352 | | | | HP:0031629 | HP:0031629 | Impaired tandem gait | 0 | PLOD1 CL E G H | 5351 | 9081 | ORPHA:1900 | Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency | HP:0040284 - Very rare | | | 105 | | | | HP:0031629 | HP:0031629 | Impaired tandem gait | 0 | SLC35C1 CL E G H | 55343 | 20197 | ORPHA:99843 | Leukocyte adhesion deficiency type II | HP:0040283 - Occasional | | | 71 | | | | HP:0031629 | HP:0031629 | Impaired tandem gait | 0 | TBC1D24 CL E G H | 57465 | 29203 | OMIM:605021 | Myoclonic epilepsy, familial infantile | | | | 271 | | |
Genes (12) :ATP6AP2 COQ5 FMR1 GDAP1 ITPR1 JAG1 KCNN2 MTRFR PCDH15 PLOD1 SLC35C1 TBC1D24
Diseases (12) :OMIM:300423 OMIM:619028 OMIM:300623 ORPHA:101097 OMIM:117360 OMIM:619574 OMIM:619724 ORPHA:254930 OMIM:602083 ORPHA:1900 ORPHA:99843 OMIM:605021 |
Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.
|
