spondyloepimetaphyseal dysplasia, di rocco type
MONDO:0060702Mondo
Findings
No curated finding names spondyloepimetaphyseal dysplasia, di rocco type yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Infantile onset
HPO, annotations 2026-09-02
Features
7 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Bowing of the legsHPOHP:0002979
- 1 of 1 reported patient
- Delayed skeletal maturationHPOHP:0002750
- 1 of 1 reported patient
- Irregular acetabular roofHPOHP:0008833
- 1 of 1 reported patient
- Metaphyseal dysplasiaHPOHP:0100255
- 1 of 1 reported patient
- Reduced bone mineral densityHPOHP:0004349
- 1 of 1 reported patient
- Short statureHPOHP:0004322
- 1 of 1 reported patient
- Waddling gaitHPOHP:0002515
- 1 of 1 reported patient
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- UFSP2HGNC:25640
- Strong · PanelApp Australia · Autosomal dominant · 2025
Where it sits
- A kind of