Disease #02878

Official abbreviation SCDO-3
Name dysostosis, spondylocostal, autosomal recessive, type 3 (SCDO-3)
OMIM ID 609813
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene LFNG
Associated tissues -
Disease features -
Remarks -