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Human Disease

spondylocostal dysostosis 3

Term ID
DOID:0112361
Synonyms
  • autosomal recessive spondylocostal dysostosis 3
  • SCDO3
Definition
A spondylocostal dysostosis that has_material_basis_in homozygous or compound heterozygous mutation in the LFNG gene on chromosome 7p22.3. https://pubmed.ncbi.nlm.nih.gov/16385447/
References
Ontology
Human Disease   ( DOID:0112361 )
Relationships
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Genes Involved
Zebrafish Models