Trait
Abnormal shape of upper motor neuron
Clinical name: Abnormal upper motor neuron morphology
Any structural anomaly that affects the upper motor neuron.
Summary
- Body system
- Abnormality of the nervous system
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page$trait$nameRead the genes linked to Abnormal shape of upper motor neuron, and the rest of your genome, with one test.
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Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Amyotrophic Lateral Sclerosis (ALS)Reads 8 of these genesALS2CHCHD10FUSSQSTM1TARDBPTBK1About this report →
- Frontotemporal DementiaReads 4 of these genesCHCHD10SQSTM1TBK1VCPAbout this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 2 of these genesTREM2TYROBPAbout this report →
- P5CS Deficiency (ALDH18A1-Related)Reads 1 of these genesALDH18A1About this report →
Show 12 more reports
- PNPLA6-Related Ataxia, Retinal Dystrophy and HypogonadismReads 1 of these genesPNPLA6About this report →
- Inherited Neurodegenerative DisordersReads 14 of these genesALS2CHCHD10ERLIN2FUSSPG7SQSTM1About this report →
- Familial Paget Disease of BoneReads 1 of these genesSQSTM1About this report →
- Hereditary Spastic ParaplegiaReads 4 of these genesERLIN2SPG7PNPLA6ALDH18A1About this report →
- Distal MyopathiesReads 2 of these genesVCPMATR3About this report →
- Alzheimer diseaseReads 1 of these genesTREM2About this report →
- Glycogen Storage DiseaseReads 1 of these genesGBE1About this report →
- Cutis LaxaReads 1 of these genesALDH18A1About this report →
- Other Inherited LeukodystrophiesReads 2 of these genesTREM2TYROBPAbout this report →
- Spinal Muscular AtrophyReads 1 of these genesCHCHD10About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesCHCHD10VCPAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesVCPAbout this report →
Read the genes linked to Abnormal shape of upper motor neuron, and the rest of your genome, with one test.
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Get my Genome Test15 genes linked to Abnormal shape of upper motor neuron
Changes in these genes cause rare conditions in which Abnormal shape of upper motor neuron is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| ALS2alsin Rho guanine nucleotide exchange factor ALS2 | Very often (80–99%) | In 3 conditions |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Very often (80–99%) | In 1 condition |
| ERLIN2ER lipid raft associated 2 | Very often (80–99%) | In 1 condition |
| FUSFUS RNA binding protein | Very often (80–99%) | In 1 condition |
| SPG7SPG7 matrix AAA peptidase subunit, paraplegin | Very often (80–99%) | In 1 condition |
| SQSTM1sequestosome 1 | Very often (80–99%) | In 1 condition |
| TARDBPTAR DNA binding protein | Very often (80–99%) | In 1 condition |
| TBK1TANK binding kinase 1 | Very often (80–99%) | In 1 condition |
| VCPvalosin containing protein | Very often (80–99%) | In 1 condition |
| PNPLA6patatin like domain 6, lysophospholipase | Sometimes (5–29%) | In 1 condition |
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Not recorded | In 1 condition |
| GBE11,4-alpha-glucan branching enzyme 1 | Not recorded | In 1 condition |
| MATR3matrin 3 | Not recorded | In 1 condition |
| TREM2triggering receptor expressed on myeloid cells 2 | Not recorded | In 1 condition |
| TYROBPtransmembrane immune signaling adaptor TYROBP | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.19-9814e911.
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