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Summary Literature (0)
MIM:123000 - CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CMDD

Xenbase Genes: ankh

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007397 - craniometaphyseal dysplasia, autosomal dominant
MONDO:0015465 - craniometaphyseal dysplasia

Disease Ontology (DO):
DOID:0080033 - craniometaphyseal dysplasia
DOID:0080801 - autosomal dominant craniometaphyseal dysplasia