Trait
Hydrocele testis
Accumulation of clear fluid in the between the layers of membrane (tunica vaginalis) surrounding the testis.
Summary
- Also called
- Testicular hydrocele
- Body system
- Abnormality of the genitourinary system
Reference genomeGRCh38hg38
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Get my Genome Test35 genes linked to Hydrocele testis
Changes in these genes cause rare conditions in which Hydrocele testis 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 |
|---|---|---|
| ADAMTS3ADAM metallopeptidase with thrombospondin type 1 motif 3 | Always | In 1 condition |
| CIROZciliated left-right organizer protein containing ZP-N domains | Always | In 1 condition |
| FRYLFRY like transcription coactivator | Always | In 1 condition |
| MECOMMDS1 and EVI1 complex locus | Always | In 1 condition |
| SLC25A10solute carrier family 25 member 10 | Always | In 1 condition |
| SOX18SRY-box transcription factor 18 | Always | In 3 conditions |
| ANGPT2angiopoietin 2 | Very often (80–99%) | In 1 condition |
| DPH2diphthamide biosynthesis 2 | Often (30–79%) | In 1 condition |
| FLT4fms related receptor tyrosine kinase 4 | Often (30–79%) | In 2 conditions |
| MDFICMyoD family inhibitor domain containing | Often (30–79%) | In 1 condition |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Often (30–79%) | In 1 condition |
| PTENphosphatase and tensin homolog | Often (30–79%) | In 2 conditions |
| SETD1ASET domain containing 1A, histone lysine methyltransferase | Often (30–79%) | In 1 condition |
| SPECC1Lsperm antigen with calponin homology and coiled-coil domains 1 like | Often (30–79%) | In 1 condition |
| THSD1thrombospondin type 1 domain containing 1 | Often (30–79%) | In 1 condition |
| VEGFCvascular endothelial growth factor C | Often (30–79%) | In 1 condition |
| ADAMTS15ADAM metallopeptidase with thrombospondin type 1 motif 15 | Sometimes (5–29%) | In 1 condition |
| CREBBPCREB binding lysine acetyltransferase | Sometimes (5–29%) | In 1 condition |
| EDEM3ER degradation enhancing alpha-mannosidase like protein 3 | Sometimes (5–29%) | In 1 condition |
| EP300EP300 lysine acetyltransferase | Sometimes (5–29%) | In 1 condition |
| FOCADfocadhesin | Sometimes (5–29%) | In 1 condition |
| KMT2Dlysine methyltransferase 2D | Sometimes (5–29%) | In 1 condition |
| MOGSmannosyl-oligosaccharide glucosidase | Sometimes (5–29%) | In 1 condition |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Sometimes (5–29%) | In 1 condition |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Sometimes (5–29%) | In 2 conditions |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Sometimes (5–29%) | In 3 conditions |
| TBX1T-box transcription factor 1 | Sometimes (5–29%) | In 1 condition |
| ZMYM2zinc finger MYM-type containing 2 | Sometimes (5–29%) | In 1 condition |
| APC2APC regulator of Wnt signaling pathway 2 | Rarely (1–4%) | In 1 condition |
| NSD1nuclear receptor binding SET domain protein 1 | Rarely (1–4%) | In 1 condition |
| ZEB2zinc finger E-box binding homeobox 2 | Rarely (1–4%) | In 2 conditions |
| ATAD3AATPase family AAA domain containing 3A | Not recorded | In 1 condition |
| EZH2enhancer of zeste 2 polycomb repressive complex 2 subunit | Not recorded | In 1 condition |
| PEX11Bperoxisomal biogenesis factor 11 beta | Not recorded | In 1 condition |
| PIEZO1piezo type mechanosensitive ion channel component 1 (Er blood group) | 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.
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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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