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Summary Literature (0)
MIM:300863 - CHONDRODYSPLASIA WITH PLATYSPONDYLY, DISTINCTIVE BRACHYDACTYLY, HYDROCEPHALY, AND MICROPHTHALMIA

Xenbase Genes: hdac6

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010463 - X-linked dominant chondrodysplasia, Chassaing-Lacombe type

Disease Ontology (DO):
DOID:0112106 - chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia