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Summary Literature (0)
MIM:617915 - HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME; HADDTS

Xenbase Genes: ctbp1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0060666 - hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome