Trait
Cornea of eye less than 10mm in diameter
Clinical name: Microcornea
A congenital abnormality of the cornea in which the cornea and the anterior segment of the eye are smaller than normal. The horizontal diameter of the cornea does not reach 10 mm even in adulthood.
Summary
- Also called
- Decreased corneal diameter
- Body system
- Abnormality of the eye
Reference genomeGRCh38hg38
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Read the genes linked to Cornea of eye less than 10mm in diameter, and the rest of your genome, with one test.
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Get my Genome Test142 genes linked to Cornea of eye less than 10mm in diameter
Changes in these genes cause rare conditions in which Cornea of eye less than 10mm in diameter 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 |
|---|---|---|
| ADAMTS18ADAM metallopeptidase with thrombospondin type 1 motif 18 | Always | In 1 condition |
| ARL2ARF like GTPase 2 | Always | In 1 condition |
| CRYBA4crystallin beta A4 | Always | In 2 conditions |
| HMGB3high mobility group box 3 | Always | In 1 condition |
| NHEJ1non-homologous end joining factor 1 | Always | In 1 condition |
| NR6A1nuclear receptor subfamily 6 group A member 1 | Always | In 1 condition |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | Always | In 2 conditions |
| RAB18RAB18, member RAS oncogene family | Always | In 2 conditions |
| TENM3teneurin transmembrane protein 3 | Always | In 1 condition |
| BCORBCL6 corepressor | Very often (80–99%) | In 4 conditions |
| CRYAAcrystallin alpha A | Very often (80–99%) | In 2 conditions |
| CRYBB1crystallin beta B1 | Very often (80–99%) | In 2 conditions |
| CRYBB2crystallin beta B2 | Very often (80–99%) | In 1 condition |
| CRYGCcrystallin gamma C | Very often (80–99%) | In 2 conditions |
| CRYGDcrystallin gamma D | Very often (80–99%) | In 1 condition |
| CTDP1CTD phosphatase 1 | Very often (80–99%) | In 2 conditions |
| FANCBFA complementation group B | Very often (80–99%) | In 1 condition |
| GJA1gap junction protein alpha 1 | Very often (80–99%) | In 3 conditions |
| GJA8gap junction protein alpha 8 | Very often (80–99%) | In 2 conditions |
| MAFMAF bZIP transcription factor | Very often (80–99%) | In 2 conditions |
| NHSNHS actin remodeling regulator | Very often (80–99%) | In 2 conditions |
| RAB3GAP1RAB3 GTPase activating protein catalytic subunit 1 | Very often (80–99%) | In 2 conditions |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Very often (80–99%) | In 2 conditions |
| TBC1D20TBC1 domain family member 20 | Very often (80–99%) | In 2 conditions |
| B3GLCTbeta 3-glucosyltransferase | Often (30–79%) | In 1 condition |
| B9D1B9 domain containing 1 | Often (30–79%) | In 1 condition |
| B9D2B9 domain containing 2 | Often (30–79%) | In 1 condition |
| BMP4bone morphogenetic protein 4 | Often (30–79%) | In 2 conditions |
| BRD4bromodomain containing 4 | Often (30–79%) | In 1 condition |
| CC2D2Acoiled-coil and C2 domain containing 2A | Often (30–79%) | In 1 condition |
| CEP290centrosomal protein 290 | Often (30–79%) | In 1 condition |
| CSPP1centrosome and spindle pole associated protein 1 | Often (30–79%) | In 1 condition |
| FAAP100FA core complex associated protein 100 | Often (30–79%) | In 1 condition |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Often (30–79%) | In 1 condition |
| HDAC8histone deacetylase 8 | Often (30–79%) | In 1 condition |
| HMX1H6 family homeobox 1 | Often (30–79%) | In 1 condition |
| MAB21L2mab-21 like 2 | Often (30–79%) | In 1 condition |
| MAU2MAU2 sister chromatid cohesion factor | Often (30–79%) | In 1 condition |
| MED25mediator complex subunit 25 | Often (30–79%) | In 2 conditions |
| MITFmelanocyte inducing transcription factor | Often (30–79%) | In 1 condition |
Show 102 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| MKS1MKS transition zone complex subunit 1 | Often (30–79%) | In 1 condition |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Often (30–79%) | In 2 conditions |
| NIPBLNIPBL cohesin loading factor | Often (30–79%) | In 2 conditions |
| PXDNperoxidasin | Often (30–79%) | In 1 condition |
| RAD21RAD21 cohesin complex component | Often (30–79%) | In 1 condition |
| RAI1retinoic acid induced 1 | Often (30–79%) | In 1 condition |
| RBSNrabenosyn, RAB effector | Often (30–79%) | In 1 condition |
| RPGRIP1RPGR interacting protein 1 | Often (30–79%) | In 1 condition |
| RPGRIP1LRPGRIP1 like | Often (30–79%) | In 1 condition |
| RSPO2R-spondin 2 | Often (30–79%) | In 1 condition |
| SC5Dsterol-C5-desaturase | Often (30–79%) | In 1 condition |
| SLC16A12solute carrier family 16 member 12 | Often (30–79%) | In 1 condition |
| SMC1Astructural maintenance of chromosomes 1A | Often (30–79%) | In 1 condition |
| SMC3structural maintenance of chromosomes 3 | Often (30–79%) | In 1 condition |
| TBL1XR1TBL1X/Y related 1 | Often (30–79%) | In 2 conditions |
| TBX4T-box transcription factor 4 | Often (30–79%) | In 1 condition |
| TCTN1tectonic family member 1 | Often (30–79%) | In 1 condition |
| TCTN2tectonic family member 2 | Often (30–79%) | In 1 condition |
| TCTN3tectonic family member 3 | Often (30–79%) | In 1 condition |
| TMEM107transmembrane protein 107 | Often (30–79%) | In 1 condition |
| TMEM216transmembrane protein 216 | Often (30–79%) | In 1 condition |
| TMEM231transmembrane protein 231 | Often (30–79%) | In 1 condition |
| TMEM237transmembrane protein 237 | Often (30–79%) | In 1 condition |
| TMEM67transmembrane protein 67 | Often (30–79%) | In 1 condition |
| TXNDC15thioredoxin domain containing 15 | Often (30–79%) | In 1 condition |
| UBE3Bubiquitin protein ligase E3B | Often (30–79%) | In 2 conditions |
| WNT3Wnt family member 3 | Often (30–79%) | In 1 condition |
| AARS1alanyl-tRNA synthetase 1 | Sometimes (5–29%) | In 1 condition |
| ACTBactin beta | Sometimes (5–29%) | In 1 condition |
| ACTG1actin gamma 1 | Sometimes (5–29%) | In 1 condition |
| ANK1ankyrin 1 | Sometimes (5–29%) | In 1 condition |
| ATOH7atonal bHLH transcription factor 7 | Sometimes (5–29%) | In 2 conditions |
| B3GALNT2beta-1,3-N-acetylgalactosaminyltransferase 2 | Sometimes (5–29%) | In 1 condition |
| B3GALT6beta-1,3-galactosyltransferase 6 | Sometimes (5–29%) | In 1 condition |
| B4GAT1beta-1,4-glucuronyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| CARS1cysteinyl-tRNA synthetase 1 | Sometimes (5–29%) | In 1 condition |
| CHN1chimerin 1 | Sometimes (5–29%) | In 1 condition |
| COL4A1collagen type IV alpha 1 chain | Sometimes (5–29%) | In 2 conditions |
| CRPPACDP-L-ribitol pyrophosphorylase A | Sometimes (5–29%) | In 1 condition |
| CTCFCCCTC-binding factor | Sometimes (5–29%) | In 1 condition |
| DAG1dystroglycan 1 | Sometimes (5–29%) | In 1 condition |
| DBR1debranching RNA lariats 1 | Sometimes (5–29%) | In 1 condition |
| DPYDdihydropyrimidine dehydrogenase | Sometimes (5–29%) | In 1 condition |
| EBPEBP cholestenol delta-isomerase | Sometimes (5–29%) | In 1 condition |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Sometimes (5–29%) | In 2 conditions |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | Sometimes (5–29%) | In 1 condition |
| FGF3fibroblast growth factor 3 | Sometimes (5–29%) | In 1 condition |
| FKRPfukutin related protein | Sometimes (5–29%) | In 1 condition |
| FKTNfukutin | Sometimes (5–29%) | In 1 condition |
| FZD4frizzled class receptor 4 | Sometimes (5–29%) | In 1 condition |
| GORABgolgin, RAB6 interacting | Sometimes (5–29%) | In 1 condition |
| GTF2E2general transcription factor IIE subunit 2 | Sometimes (5–29%) | In 2 conditions |
| GTF2H5general transcription factor IIH subunit 5 | Sometimes (5–29%) | In 1 condition |
| HSPG2heparan sulfate proteoglycan 2 | Sometimes (5–29%) | In 2 conditions |
| KDM6Alysine demethylase 6A | Sometimes (5–29%) | In 1 condition |
| KMT2Dlysine methyltransferase 2D | Sometimes (5–29%) | In 1 condition |
| LARGE1LARGE xylosyl- and glucuronyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| MAFBMAF bZIP transcription factor B | Sometimes (5–29%) | In 1 condition |
| MAPRE2microtubule associated protein RP/EB family member 2 | Sometimes (5–29%) | In 2 conditions |
| MED16mediator complex subunit 16 | Sometimes (5–29%) | In 1 condition |
| MPLKIPM-phase specific PLK1 interacting protein | Sometimes (5–29%) | In 2 conditions |
| NDPnorrin cystine knot growth factor NDP | Sometimes (5–29%) | In 1 condition |
| PAX6paired box 6 | Sometimes (5–29%) | In 2 conditions |
| PLK4polo like kinase 4 | Sometimes (5–29%) | In 1 condition |
| POMGNT1protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Sometimes (5–29%) | In 1 condition |
| POMGNT2protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) | Sometimes (5–29%) | In 1 condition |
| POMKprotein O-mannose kinase | Sometimes (5–29%) | In 1 condition |
| POMT1protein O-mannosyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| POMT2protein O-mannosyltransferase 2 | Sometimes (5–29%) | In 1 condition |
| PORCNporcupine O-acyltransferase | Sometimes (5–29%) | In 1 condition |
| PRR12proline rich 12 | Sometimes (5–29%) | In 1 condition |
| PRSS56serine protease 56 | Sometimes (5–29%) | In 1 condition |
| PYCR1pyrroline-5-carboxylate reductase 1 | Sometimes (5–29%) | In 1 condition |
| RBP4retinol binding protein 4 | Sometimes (5–29%) | In 1 condition |
| RNF113Aring finger protein 113A | Sometimes (5–29%) | In 1 condition |
| RXYLT1ribitol xylosyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| SALL4spalt like transcription factor 4 | Sometimes (5–29%) | In 2 conditions |
| TARS1threonyl-tRNA synthetase 1 | Sometimes (5–29%) | In 1 condition |
| TBX22T-box transcription factor 22 | Sometimes (5–29%) | In 1 condition |
| TFAP2Atranscription factor AP-2 alpha | Sometimes (5–29%) | In 1 condition |
| TSHZ3teashirt zinc finger homeobox 3 | Sometimes (5–29%) | In 1 condition |
| TUBBtubulin beta class I | Sometimes (5–29%) | In 2 conditions |
| ZEB2zinc finger E-box binding homeobox 2 | Sometimes (5–29%) | In 2 conditions |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Rarely (1–4%) | In 2 conditions |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Rarely (1–4%) | In 1 condition |
| FKBP14FKBP prolyl isomerase 14 | Rarely (1–4%) | In 1 condition |
| BEST1bestrophin 1 | Not recorded | In 1 condition |
| CENPFcentromere protein F | Not recorded | In 1 condition |
| CHST14carbohydrate sulfotransferase 14 | Not recorded | In 1 condition |
| FOXE3forkhead box E3 | Not recorded | In 1 condition |
| FOXL2forkhead box L2 | Not recorded | In 1 condition |
| JAG1jagged canonical Notch ligand 1 | Not recorded | In 1 condition |
| KIF11kinesin family member 11 | Not recorded | In 1 condition |
| KRASKRas proto-oncogene, GTPase | Not recorded | In 1 condition |
| LMX1BLIM homeobox transcription factor 1 beta | Not recorded | In 1 condition |
| MIR184microRNA 184 | Not recorded | In 1 condition |
| OTX2orthodenticle homeobox 2 | Not recorded | In 1 condition |
| PITX2paired like homeodomain 2 | Not recorded | In 1 condition |
| PITX3paired like homeodomain 3 | Not recorded | In 1 condition |
| RAB23RAB23, member RAS oncogene family | Not recorded | In 1 condition |
| RECQL4RecQ like helicase 4 | Not recorded | In 1 condition |
| TBX15T-box transcription factor 15 | 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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