Disease #02781 (SCDO-2 (dysostosis, spondylocostal, autosomal recessive, type 2 (SCDO-2)), OMIM:608681)

Official abbreviation SCDO-2
Name dysostosis, spondylocostal, autosomal recessive, type 2 (SCDO-2)
OMIM ID 608681
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MESP2
Associated tissues -
Disease features -
Remarks -