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Trait
Abnormal cortical bone morphology
An abnormality of compact bone (also known as cortical bone), which forms the dense surface of bones.
Summary
- Also called
- Abnormal compact bone morphology, Abnormality of cortical bone
- Body system
- Abnormality of the musculoskeletal system
Abnormal cortical bone morphologyHP:0003103
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Read the genes linked to Abnormal cortical bone morphology, and the rest of your genome, with one test.
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Get my Genome Test49 genes linked to Abnormal cortical bone morphology
Changes in these genes cause rare conditions in which Abnormal cortical bone 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 |
|---|---|---|
| FLNAfilamin A | Very often (80–99%) | In 1 condition |
| HPGD15-hydroxyprostaglandin dehydrogenase | Very often (80–99%) | In 2 conditions |
| KIF1Akinesin family member 1A | Very often (80–99%) | In 1 condition |
| LEMD3LEM domain containing 3 | Very often (80–99%) | In 1 condition |
| LIFRLIF receptor subunit alpha | Very often (80–99%) | In 1 condition |
| LRP4LDL receptor related protein 4 | Very often (80–99%) | In 1 condition |
| LRP5LDL receptor related protein 5 | Very often (80–99%) | In 2 conditions |
| PTDSS1phosphatidylserine synthase 1 | Very often (80–99%) | In 1 condition |
| RETREG1reticulophagy regulator 1 | Very often (80–99%) | In 1 condition |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Very often (80–99%) | In 1 condition |
| SLCO2A1solute carrier organic anion transporter family member 2A1 | Very often (80–99%) | In 1 condition |
| SOSTsclerostin | Very often (80–99%) | In 2 conditions |
| TBXAS1thromboxane A synthase 1 | Very often (80–99%) | In 1 condition |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Very often (80–99%) | In 1 condition |
| WNK1WNK lysine deficient protein kinase 1 | Very often (80–99%) | In 1 condition |
| AGAaspartylglucosaminidase | Often (30–79%) | In 1 condition |
| ANKLE2ankyrin repeat and LEM domain containing 2 | Often (30–79%) | In 1 condition |
| ASPMassembly factor for spindle microtubules | Often (30–79%) | In 1 condition |
| CDK5RAP2CDK5 regulatory subunit associated protein 2 | Often (30–79%) | In 1 condition |
| CDK6cyclin dependent kinase 6 | Often (30–79%) | In 1 condition |
| CENPEcentromere protein E | Often (30–79%) | In 1 condition |
| CEP135centrosomal protein 135 | Often (30–79%) | In 1 condition |
| CEP152centrosomal protein 152 | Often (30–79%) | In 1 condition |
| CITcitron rho-interacting serine/threonine kinase | Often (30–79%) | In 1 condition |
| COPB2coat protein complex I subunit beta 2 | Often (30–79%) | In 1 condition |
| CPAPcentrosome assembly and centriole elongation protein | Often (30–79%) | In 1 condition |
| GJA1gap junction protein alpha 1 | Often (30–79%) | In 1 condition |
| GLE1GLE1 RNA export mediator | Often (30–79%) | In 1 condition |
| KIF14kinesin family member 14 | Often (30–79%) | In 1 condition |
| KNL1kinetochore scaffold 1 | Often (30–79%) | In 1 condition |
| MCM7minichromosome maintenance complex component 7 | Often (30–79%) | In 1 condition |
| MCPH1microcephalin 1 | Often (30–79%) | In 1 condition |
| METTL5methyltransferase 5, N6-adenosine | Often (30–79%) | In 1 condition |
| MFSD2AMFSD2 lysolipid transporter A, lysophospholipid | Often (30–79%) | In 1 condition |
| NCAPD3non-SMC condensin II complex subunit D3 | Often (30–79%) | In 1 condition |
| NUP37nucleoporin 37 | Often (30–79%) | In 1 condition |
| PDCD6IPprogrammed cell death 6 interacting protein | Often (30–79%) | In 1 condition |
| PHC1polyhomeotic homolog 1 | Often (30–79%) | In 1 condition |
| PYCR2pyrroline-5-carboxylate reductase 2 | Often (30–79%) | In 1 condition |
| SARS1seryl-tRNA synthetase 1 | Often (30–79%) | In 1 condition |
Show 9 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| SASS6SAS-6 centriolar assembly protein | Often (30–79%) | In 1 condition |
| STILSTIL centriolar assembly protein | Often (30–79%) | In 1 condition |
| TAF13TATA-box binding protein associated factor 13 | Often (30–79%) | In 1 condition |
| TRAPPC10trafficking protein particle complex subunit 10 | Often (30–79%) | In 1 condition |
| TRAPPC14trafficking protein particle complex subunit 14 | Often (30–79%) | In 1 condition |
| WARS1tryptophanyl-tRNA synthetase 1 | Often (30–79%) | In 1 condition |
| WDR62WD repeat domain 62 | Often (30–79%) | In 1 condition |
| NSDHLNAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL | Not recorded | In 1 condition |
| PEX19peroxisomal biogenesis factor 19 | 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
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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