Rare diseases · Sign or symptom
Congenital hip dislocation
Dislocated hip since birth
HP:0001374
Rare diseases that can present with this33
Common30–79%
5Sometimes5–29%
16- 17p13.3microduplication syndrome
- 19q13.11microdeletion syndrome
- 3M syndrome
- 8q24.3microdeletion syndrome
- Alacrimia-choreoathetosis-liver dysfunction syndrome
- Autosomal recessive cutis laxa type 2A
- Brittle cornea syndrome
- Congenital fiber-type disproportion myopathy
and 8 more in this range
Rare1–4%
8- Congenital myasthenic syndrome
- Dextrocardia
- Dysplasia of head of femur, Meyer type
- Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome
- Houge-Janssens syndrome type 1
- Isolated radio-ulnar synostosis
- Presynaptic congenital myasthenic syndrome
- Sjögren-Larsson syndrome
The range is how often this sign appears among people diagnosed with each disease — it is not a probability of having any of them. Many of these signs also occur in common, non-rare conditions. A sign on this page is a conversation to have with a clinician, not a conclusion.
Part of the broader category
Also called: Congenital dislocation of the hip · Congenital dislocation of the hips · Congenital hip anomaly · Congenital hip dislocations
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Start free with EleplanThis page uses the Human Phenotype Ontology (2026-06-23) — Human Phenotype Ontology Consortium, hpo.jax.org. Disease associations from Orphanet (INSERM), CC BY 4.0. Content is educational and is not medical advice.