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Human Disease

spondylocostal dysostosis 6

Term ID
DOID:0112360
Synonyms
  • autosomal recessive spondylocostal dysostosis 6
  • SCDO6
Definition
A spondylocostal dysostosis that has_material_basis_in homozygous or compound heterozygous mutation in the RIPPLY2 gene on chromosome 6q14.2. https://pubmed.ncbi.nlm.nih.gov/25343988/
References
Ontology
Human Disease   ( DOID:0112360 )
Relationships
is a type of
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Genes Involved
Zebrafish Models