/craniodiaphyseal dysplasia, autosomal dominant

craniodiaphyseal dysplasia, autosomal dominant

Rare Disease

MONDO:0021021

Also Known As

CDDcraniodiaphyseal dysplasia, autosomal dominantSchaefer Stein Oshman syndromecraniodiaphyseal dysplasia, dominantdominantly inherited craniodiaphyseal dysplasia

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Associated Genes

SOST ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:122860 ↗

GARD

GARD:249 ↗

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