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Summary Literature (0)
MIM:617330 - HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS

Xenbase Genes: ebf3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0015021 - hypotonia, ataxia, and delayed development syndrome

Disease Ontology (DO):
DOID:0081176 - hypotonia, ataxia, and delayed development syndrome