spondylocostal dysostosis 6, autosomal recessive
Findings
No curated finding names spondylocostal dysostosis 6, autosomal recessive yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any autosomal recessive spondylocostal dysostosis in which the cause of the disease is a mutation in the RIPPLY2 gene.
Definition from the Mondo Disease Ontology (MONDO:0014694), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal recessive inheritance
HPO, annotations 2026-09-02
Features
5 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.
- HemivertebraeHPOHP:0002937
- 2 of 2 reported patients
- Butterfly vertebraeHPOHP:0003316
- 1 of 2 reported patients
- Cervical kyphosisHPOHP:0002947
- 1 of 2 reported patients
- ScoliosisHPOHP:0002650
- 1 of 2 reported patients
- Spinal canal stenosisHPOHP:0003416
- 1 of 2 reported patients
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.
- RIPPLY2HGNC:21390
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2019
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Limited · Ambry Genetics · Autosomal recessive · 2020
- Limited · Labcorp Genetics (formerly Invitae) · Unknown · 2021
Where it sits
Other names
2 names
Resolves to: spondylocostal dysostosis 6, autosomal recessive
- Also called
- autosomal recessive spondylocostal dysostosis caused by mutation in RIPPLY2RIPPLY2 autosomal recessive spondylocostal dysostosis