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Summary Literature (0)
MIM:616579 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, IMPAIRED LANGUAGE, AND DYSMORPHIC FEATURES; NEDHILD

Xenbase Genes: champ1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014699 - intellectual disability, autosomal dominant 40
MONDO:0100172 - intellectual disability, autosomal dominant

Disease Ontology (DO):
DOID:0070070 - autosomal dominant intellectual developmental disorder 40