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Trait
Dysgraphia
A writing disability in the absence of motor or sensory deficits of the upper extremities, resulting in an impairment in the ability to write regardless of the ability to read and not due to intellectual impairment.
Summary
- Body system
- Abnormality of the nervous system
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This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/dysgraphia.json"
page <- fromJSON(url)
page$trait$nameDysgraphiaHP:0010526
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Get my Genome Test44 condition reports read genes linked to this trait
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.
- Lynch SyndromeReads 5 of these genesEPCAMMLH1MSH2MSH6PMS2About this report →
- Alzheimer diseaseReads 4 of these genesPSEN1TREM2APPPSEN2About this report →
- Frontotemporal DementiaReads 6 of these genesCHMP2BGRNMAPTPSEN1SQSTM1VCPAbout this report →
- Colorectal Cancer & PolyposisReads 3 of these genesMUTYHPOLD1POLEAbout this report →
Show 40 more reports
- Ataxia-TelangiectasiaReads 1 of these genesATMAbout this report →
- MDPL SyndromeReads 1 of these genesPOLD1About this report →
- DNA Repair DiseaseReads 5 of these genesBRCA2MLH1MSH2MSH6PMS2About this report →
- Inherited Neurodegenerative DisordersReads 14 of these genesCHMP2BGRNMAPTPSEN1SQSTM1TMEM106BAbout this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 1 of these genesBRCA2About this report →
- Hereditary Mixed Polyposis SyndromeReads 1 of these genesBMPR1AAbout this report →
- Juvenile Polyposis SyndromeReads 1 of these genesBMPR1AAbout this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 2 of these genesATMCHEK2About this report →
- Cerebral Amyloid AngiopathyReads 1 of these genesAPPAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 3 of these genesCHMP2BSQSTM1VCPAbout this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 1 of these genesTREM2About this report →
- Familial Paget Disease of BoneReads 1 of these genesSQSTM1About this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFBR2About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 2 of these genesTMEM240FGF14About this report →
- Marfan Like SyndromesReads 1 of these genesTGFBR2About this report →
- Hereditary AmyloidosisReads 1 of these genesAPPAbout this report →
- Aortic AneurysmReads 1 of these genesTGFBR2About this report →
- Congenital Diarrhoeas & EnteropathiesReads 1 of these genesEPCAMAbout this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Other Inborn Errors of ImmunityReads 4 of these genesNCF1ATMKRASPOLD1About this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesGRNAbout this report →
- Parkinson DiseaseReads 1 of these genesMAPTAbout this report →
- Cutis LaxaReads 1 of these genesELNAbout this report →
- Fanconi AnemiaReads 1 of these genesBRCA2About this report →
- Distal MyopathiesReads 1 of these genesVCPAbout this report →
- Other Inherited LeukodystrophiesReads 2 of these genesTMEM106BTREM2About this report →
- Autoimmune DiseaseReads 1 of these genesKRASAbout this report →
- Noonan SyndromeReads 1 of these genesKRASAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesTMEM106BAbout this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Female InfertilityReads 1 of these genesATMAbout this report →
- Lysosomal Storage DiseaseReads 1 of these genesGRNAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesKRASAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesSPG21About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesVCPAbout this report →
- Primary Mitochondrial DiseaseReads 1 of these genesDNAJC30About this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesVCPAbout this report →
Read the genes linked to Dysgraphia, and the rest of your genome, with one test.
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Get my Genome Test54 genes linked to Dysgraphia
Changes in these genes cause rare conditions in which Dysgraphia 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 |
|---|---|---|
| LRRC7leucine rich repeat containing 7 | Always | In 1 condition |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Very often (80–99%) | In 1 condition |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Very often (80–99%) | In 1 condition |
| CHMP2Bcharged multivesicular body protein 2B | Very often (80–99%) | In 3 conditions |
| CLIP2CAP-Gly domain containing linker protein 2 | Very often (80–99%) | In 1 condition |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Very often (80–99%) | In 1 condition |
| EIF4Heukaryotic translation initiation factor 4H | Very often (80–99%) | In 1 condition |
| ELNelastin | Very often (80–99%) | In 1 condition |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Very often (80–99%) | In 1 condition |
| GRNgranulin precursor | Very often (80–99%) | In 3 conditions |
| GTF2Igeneral transcription factor IIi | Very often (80–99%) | In 1 condition |
| GTF2IRD1GTF2I repeat domain containing 1 | Very often (80–99%) | In 1 condition |
| GTF2IRD2GTF2I repeat domain containing 2 | Very often (80–99%) | In 1 condition |
| LIMK1LIM domain kinase 1 | Very often (80–99%) | In 1 condition |
| MAPTmicrotubule associated protein tau | Very often (80–99%) | In 3 conditions |
| METTL27methyltransferase like 27 | Very often (80–99%) | In 1 condition |
| NCF1neutrophil cytosolic factor 1 | Very often (80–99%) | In 1 condition |
| PSEN1presenilin 1 | Very often (80–99%) | In 4 conditions |
| RFC2replication factor C subunit 2 | Very often (80–99%) | In 1 condition |
| SQSTM1sequestosome 1 | Very often (80–99%) | In 1 condition |
| STX1Asyntaxin 1A | Very often (80–99%) | In 1 condition |
| TBL2transducin beta like 2 | Very often (80–99%) | In 1 condition |
| TMEM106Btransmembrane protein 106B | Very often (80–99%) | In 3 conditions |
| TMEM270transmembrane protein 270 | Very often (80–99%) | In 1 condition |
| TREM2triggering receptor expressed on myeloid cells 2 | Very often (80–99%) | In 4 conditions |
| VCPvalosin containing protein | Very often (80–99%) | In 2 conditions |
| VPS37DVPS37D subunit of ESCRT-I | Very often (80–99%) | In 1 condition |
| SPG21SPG21 abhydrolase domain containing, maspardin | Often (30–79%) | In 1 condition |
| TMEM240transmembrane protein 240 | Often (30–79%) | In 2 conditions |
| APPamyloid beta precursor protein | Sometimes (5–29%) | In 1 condition |
| ATMATM serine/threonine kinase | Sometimes (5–29%) | In 1 condition |
| BMPR1Abone morphogenetic protein receptor type 1A | Sometimes (5–29%) | In 1 condition |
| BRCA2BRCA2 DNA repair associated | Sometimes (5–29%) | In 1 condition |
| CHEK2checkpoint kinase 2 | Sometimes (5–29%) | In 1 condition |
| EPCAMepithelial cell adhesion molecule | Sometimes (5–29%) | In 1 condition |
| KRASKRas proto-oncogene, GTPase | Sometimes (5–29%) | In 1 condition |
| MLH1mutL homolog 1 | Sometimes (5–29%) | In 1 condition |
| MSH2mutS homolog 2 | Sometimes (5–29%) | In 1 condition |
| MSH6mutS homolog 6 | Sometimes (5–29%) | In 1 condition |
| MUTYHmutY DNA glycosylase | Sometimes (5–29%) | In 1 condition |
Show 14 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| NPATnuclear protein, coactivator of histone transcription | Sometimes (5–29%) | In 1 condition |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Sometimes (5–29%) | In 1 condition |
| PMS1PMS1 homolog 1, mismatch repair system component | Sometimes (5–29%) | In 1 condition |
| PMS2PMS1 homolog 2, mismatch repair system component | Sometimes (5–29%) | In 1 condition |
| POLD1DNA polymerase delta 1, catalytic subunit | Sometimes (5–29%) | In 1 condition |
| POLEDNA polymerase epsilon, catalytic subunit | Sometimes (5–29%) | In 1 condition |
| PSEN2presenilin 2 | Sometimes (5–29%) | In 1 condition |
| RPS20ribosomal protein S20 | Sometimes (5–29%) | In 1 condition |
| SEMA4Asemaphorin 4A | Sometimes (5–29%) | In 1 condition |
| SORL1sortilin related receptor 1 | Sometimes (5–29%) | In 1 condition |
| SOX6SRY-box transcription factor 6 | Sometimes (5–29%) | In 1 condition |
| TGFBR2transforming growth factor beta receptor 2 | Sometimes (5–29%) | In 1 condition |
| TOMM40translocase of outer mitochondrial membrane 40 | Sometimes (5–29%) | In 1 condition |
| FGF14fibroblast growth factor 14 | Rarely (1–4%) | 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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