Trait
Thin bony cortex
Abnormal thinning of the cortical region of bones.
Summary
- Also called
- Thin cortices
- Body system
- Abnormality of the musculoskeletal system
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Thin bony cortex, and the rest of your genome, with one test.
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Get my Genome Test24 genes linked to Thin bony cortex
Changes in these genes cause rare conditions in which Thin bony cortex 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 |
|---|---|---|
| ANKHANKH inorganic pyrophosphate transport regulator | Always | In 1 condition |
| CCDC134coiled-coil domain containing 134 | Always | In 1 condition |
| FARSBphenylalanyl-tRNA synthetase subunit beta | Always | In 1 condition |
| GLB1galactosidase beta 1 | Always | In 1 condition |
| MMP2matrix metallopeptidase 2 | Always | In 1 condition |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Always | In 1 condition |
| SERPINH1serpin family H member 1 | Always | In 1 condition |
| SFRP4secreted frizzled related protein 4 | Always | In 1 condition |
| SMSspermine synthase | Always | In 1 condition |
| TMEM38Btransmembrane protein 38B | Always | In 1 condition |
| CYP27B1cytochrome P450 family 27 subfamily B member 1 | Very often (80–99%) | In 2 conditions |
| CYP2R1cytochrome P450 family 2 subfamily R member 1 | Very often (80–99%) | In 2 conditions |
| TMEM53transmembrane protein 53 | Very often (80–99%) | In 1 condition |
| PRKG2protein kinase cGMP-dependent 2 | Often (30–79%) | In 1 condition |
| PTH1Rparathyroid hormone 1 receptor | Often (30–79%) | In 2 conditions |
| XYLT2xylosyltransferase 2 | Often (30–79%) | In 1 condition |
| ADAMTS10ADAM metallopeptidase with thrombospondin type 1 motif 10 | Not recorded | In 1 condition |
| AKT1AKT serine/threonine kinase 1 | Not recorded | In 1 condition |
| CLCN5Cl-/H+ antiporter 5 | Not recorded | In 2 conditions |
| FBN1fibrillin 1 | Not recorded | In 1 condition |
| SLC34A3solute carrier family 34 member 3 | Not recorded | In 1 condition |
| TENT5Aterminal nucleotidyltransferase 5A | Not recorded | In 1 condition |
| TNFRSF11ATNF receptor superfamily member 11a | Not recorded | In 1 condition |
| VDRvitamin D receptor | 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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