Trait

Congenital bilateral hip dislocation

Body system: Abnormality of limbs Abnormality of the musculoskeletal system

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10 genes linked to Congenital bilateral hip dislocation

Changes in these genes cause rare conditions in which Congenital bilateral hip dislocation 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
COL1A1collagen type I alpha 1 chain	Always	In 2 conditions
COL1A2collagen type I alpha 2 chain	Very often (80–99%)	In 1 condition
FBLN1fibulin 1	Often (30–79%)	In 1 condition
SHROOM4shroom family member 4	Often (30–79%)	In 1 condition
VIPAS39VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog	Often (30–79%)	In 1 condition
VPS33BVPS33B late endosome and lysosome associated	Often (30–79%)	In 1 condition
CLTCL1clathrin heavy chain like 1	Sometimes (5–29%)	In 1 condition
COL12A1collagen type XII alpha 1 chain	Sometimes (5–29%)	In 1 condition
PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1	Sometimes (5–29%)	In 1 condition
TELO2telomere maintenance 2	Sometimes (5–29%)	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

Dislocated hip since birth

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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