Trait
Chordee
A congenital anomaly of the penis characterized by ventral (i.e., downward), lateral, or ventrolateral curvature of the shaft and glans penis of more than 30 degrees.
Summary
- Body system
- Abnormality of the genitourinary system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Get my Genome Test24 genes linked to Chordee
Changes in these genes cause rare conditions in which Chordee 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 |
|---|---|---|
| EIF4A2eukaryotic translation initiation factor 4A2 | Always | In 1 condition |
| FRYLFRY like transcription coactivator | Always | In 1 condition |
| MYH3myosin heavy chain 3 | Always | In 1 condition |
| REREarginine-glutamic acid dipeptide repeats | Always | In 1 condition |
| BBS2Bardet-Biedl syndrome 2 | Often (30–79%) | In 1 condition |
| KDM1Alysine demethylase 1A | Often (30–79%) | In 2 conditions |
| PPP1R12Aprotein phosphatase 1 regulatory subunit 12A | Often (30–79%) | In 1 condition |
| CDC42BPBCDC42 binding protein kinase beta | Sometimes (5–29%) | In 1 condition |
| DOT1LDOT1 like histone lysine methyltransferase | Sometimes (5–29%) | In 1 condition |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Sometimes (5–29%) | In 1 condition |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Sometimes (5–29%) | In 1 condition |
| SRYsex determining region Y | Sometimes (5–29%) | In 1 condition |
| ZMYM2zinc finger MYM-type containing 2 | Sometimes (5–29%) | In 1 condition |
| ZNF699zinc finger protein 699 | Sometimes (5–29%) | In 1 condition |
| ZEB2zinc finger E-box binding homeobox 2 | Rarely (1–4%) | In 2 conditions |
| CARS1cysteinyl-tRNA synthetase 1 | Not recorded | In 1 condition |
| COX7Bcytochrome c oxidase subunit 7B | Not recorded | In 1 condition |
| FGFR1fibroblast growth factor receptor 1 | Not recorded | In 1 condition |
| HCCSholocytochrome c synthase | Not recorded | In 1 condition |
| HOXA13homeobox A13 | Not recorded | In 1 condition |
| MAP3K1mitogen-activated protein kinase kinase kinase 1 | Not recorded | In 1 condition |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Not recorded | In 1 condition |
| PORcytochrome p450 oxidoreductase | Not recorded | In 1 condition |
| PTDSS1phosphatidylserine synthase 1 | 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 2026.10.16-c6eea6bf.
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