Trait
Abnormal enchondral ossification
An abnormality of the process of endochondral ossification, which is a type of replacement ossification in which bone tissue replaces cartilage.
Summary
- Body system
- Abnormality of the musculoskeletal system
Reference genomeGRCh38hg38
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Changes in these genes cause rare conditions in which Abnormal enchondral ossification 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.
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
- Abnormal bone maturation of vertebra14 genes
- Abnormal maturation of the pelvis bone7 genes
- Abnormal maturation of breastbone5 genes
- Abnormal maturation of thigh bone head and neck4 genes
- Abnormal foot bone ossification2 genes
- Abnormal maturation of the hand bones2 genes
- Delayed bone maturation of the knee cap2 genes
- Abnormal maturation of the end part of a bone1 gene
- Calcific stippling of infantile cartilaginous skeleton1 gene
- Abnormal maturation of long bone in upper arm
- Abnormal maturation of rib bones
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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