OBO ID: DOID:0112361
Term Name: spondylocostal dysostosis 3 Search Ontology:
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
is a type of:
OTHER spondylocostal dysostosis 3 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
LFNG Spondylocostal dysostosis 3, autosomal recessive 609813
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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