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DO Term : spondylocostal dysostosis 2 [DOID:0112362] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A spondylocostal dysostosis that has_material_basis_in homozygous or compound heterozygous mutation in the MESP2 gene on chromosome 15q26.1.

synonyms:
GARD:6798,
autosomal recessive spondylocostal dysostosis 2,
SCDO2,
608681,
OMIM:608681

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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