Trait
Developmental glaucoma
Glaucoma which forms during the early years of a child's life is called developmental or congenital glaucoma.
Summary
- Also called
- Childhood glaucoma, Infantile glaucoma, Paediatric glaucoma, Pediatric glaucoma
- Body system
- Abnormality of the eye
Reference genomeGRCh38hg38
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Get my Genome Test51 genes linked to Developmental glaucoma
Changes in these genes cause rare conditions in which Developmental glaucoma 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 |
|---|---|---|
| PYCR1pyrroline-5-carboxylate reductase 1 | Always | In 1 condition |
| FOXE3forkhead box E3 | Very often (80–99%) | In 2 conditions |
| CYP1B1cytochrome P450 family 1 subfamily B member 1 | Often (30–79%) | In 2 conditions |
| FOXC1forkhead box C1 | Often (30–79%) | In 1 condition |
| PAX6paired box 6 | Often (30–79%) | In 1 condition |
| PITX2paired like homeodomain 2 | Often (30–79%) | In 1 condition |
| SH3PXD2BSH3 and PX domains 2B | Often (30–79%) | In 1 condition |
| ADARadenosine deaminase RNA specific | Sometimes (5–29%) | In 1 condition |
| FLNAfilamin A | Sometimes (5–29%) | In 1 condition |
| IFIH1interferon induced with helicase C domain 1 | Sometimes (5–29%) | In 1 condition |
| LSM11LSM11, U7 small nuclear RNA associated | Sometimes (5–29%) | In 1 condition |
| MAFAMAF bZIP transcription factor A | Sometimes (5–29%) | In 1 condition |
| PTBP1polypyrimidine tract binding protein 1 | Sometimes (5–29%) | In 1 condition |
| RNASEH2Aribonuclease H2 subunit A | Sometimes (5–29%) | In 1 condition |
| RNASEH2Bribonuclease H2 subunit B | Sometimes (5–29%) | In 1 condition |
| RNASEH2Cribonuclease H2 subunit C | Sometimes (5–29%) | In 1 condition |
| RNU7-1RNA, U7 small nuclear 1 | Sometimes (5–29%) | In 1 condition |
| SAMHD1SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 | Sometimes (5–29%) | In 1 condition |
| SBF2SET binding factor 2 | Sometimes (5–29%) | In 1 condition |
| SRYsex determining region Y | Sometimes (5–29%) | In 1 condition |
| TREX1three prime repair exonuclease 1 | Sometimes (5–29%) | In 1 condition |
| ADA2adenosine deaminase 2 | Rarely (1–4%) | In 1 condition |
| GATA1GATA binding protein 1 | Rarely (1–4%) | In 1 condition |
| HEATR3HEAT repeat containing 3 | Rarely (1–4%) | In 1 condition |
| RPL11ribosomal protein L11 | Rarely (1–4%) | In 1 condition |
| RPL15ribosomal protein L15 | Rarely (1–4%) | In 1 condition |
| RPL18ribosomal protein L18 | Rarely (1–4%) | In 1 condition |
| RPL26ribosomal protein L26 | Rarely (1–4%) | In 1 condition |
| RPL27ribosomal protein L27 | Rarely (1–4%) | In 1 condition |
| RPL31ribosomal protein L31 | Rarely (1–4%) | In 1 condition |
| RPL35ribosomal protein L35 | Rarely (1–4%) | In 1 condition |
| RPL35Aribosomal protein L35a | Rarely (1–4%) | In 1 condition |
| RPL5ribosomal protein L5 | Rarely (1–4%) | In 1 condition |
| RPL8ribosomal protein L8 | Rarely (1–4%) | In 1 condition |
| RPL9ribosomal protein L9 | Rarely (1–4%) | In 1 condition |
| RPS10ribosomal protein S10 | Rarely (1–4%) | In 1 condition |
| RPS15Aribosomal protein S15a | Rarely (1–4%) | In 1 condition |
| RPS17ribosomal protein S17 | Rarely (1–4%) | In 1 condition |
| RPS19ribosomal protein S19 | Rarely (1–4%) | In 1 condition |
| RPS20ribosomal protein S20 | Rarely (1–4%) | In 1 condition |
Show 11 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| RPS24ribosomal protein S24 | Rarely (1–4%) | In 1 condition |
| RPS26ribosomal protein S26 | Rarely (1–4%) | In 1 condition |
| RPS27ribosomal protein S27 | Rarely (1–4%) | In 1 condition |
| RPS28ribosomal protein S28 | Rarely (1–4%) | In 1 condition |
| RPS29ribosomal protein S29 | Rarely (1–4%) | In 1 condition |
| RPS7ribosomal protein S7 | Rarely (1–4%) | In 1 condition |
| TSR2TSR2 ribosome maturation factor | Rarely (1–4%) | In 1 condition |
| B3GAT3beta-1,3-glucuronyltransferase 3 | Not recorded | In 1 condition |
| CANT1calcium activated nucleotidase 1 | Not recorded | In 1 condition |
| CHST3carbohydrate sulfotransferase 3 | Not recorded | In 1 condition |
| GLIS3GLIS family zinc finger 3 | 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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