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DO Term : spondylocostal dysostosis 6 [DOID:0112360] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A spondylocostal dysostosis that has_material_basis_in homozygous or compound heterozygous mutation in the RIPPLY2 gene on chromosome 6q14.2.

synonyms:
OMIM:616566,
SCDO6,
autosomal recessive spondylocostal dysostosis 6,
616566

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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