Trait
Abnormal cornea morphology
Any abnormality of the cornea, which is the transparent tissue at the front of the eye that covers the iris, pupil, and anterior chamber.
Summary
- Also called
- Abnormality of the cornea, Corneal abnormalities, Corneal abnormality
- Body system
- Abnormality of the eye
Reference genomeGRCh38hg38
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Read the genes linked to Abnormal cornea morphology, and the rest of your genome, with one test.
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Get my Genome Test15 genes linked to Abnormal cornea morphology
Changes in these genes cause rare conditions in which Abnormal cornea morphology 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 |
|---|---|---|
| CTNScystinosin, lysosomal cystine transporter | Very often (80–99%) | In 2 conditions |
| TGFBItransforming growth factor beta induced | Very often (80–99%) | In 1 condition |
| MEGF8multiple EGF like domains 8 | Often (30–79%) | In 1 condition |
| RAB23RAB23, member RAS oncogene family | Often (30–79%) | In 1 condition |
| COL1A1collagen type I alpha 1 chain | Sometimes (5–29%) | In 1 condition |
| COL5A1collagen type V alpha 1 chain | Sometimes (5–29%) | In 1 condition |
| COL5A2collagen type V alpha 2 chain | Sometimes (5–29%) | In 1 condition |
| FLNAfilamin A | Sometimes (5–29%) | In 1 condition |
| LAMA3laminin subunit alpha 3 | Sometimes (5–29%) | In 1 condition |
| LAMB3laminin subunit beta 3 | Sometimes (5–29%) | In 1 condition |
| LAMC2laminin subunit gamma 2 | Sometimes (5–29%) | In 1 condition |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Sometimes (5–29%) | In 1 condition |
| DNAI1dynein axonemal intermediate chain 1 | Not recorded | In 1 condition |
| PITX2paired like homeodomain 2 | Not recorded | In 1 condition |
| ZNF469zinc finger protein 469 | 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.
Narrower traits
- Corneal opacity166 genes
- Corneal dystrophy33 genes
- New blood vessel formation in cornea27 genes
- Abnormal corneal endothelium morphology15 genes
- Corneal perforation14 genes
- Benign eye tumor9 genes
- Abnormal corneal limbus morphology2 genes
- Abnormal corneal epithelium morphology1 gene
- Cornea verticillata1 gene
- Corneal degeneration1 gene
- Corneopalpebral synechiae1 gene
- Abnormal corneal stroma morphology
- Abnormal corneal thickness
- Abnormal line of Schwalbe morphology
- Abnormality of corneal size
- Abnormality of the curvature of the cornea
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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