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Summary Literature (0)
MIM:615866 - INTELLECTUAL DEVELOPMENTAL DISORDER WITH MICROCEPHALY AND WITH OR WITHOUT OCULAR MALFORMATIONS OR HYPOGONADOTROPIC HYPOGONADISM; IDDMOH

Xenbase Genes: sox11

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014376 - intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism
MONDO:0015452 - Coffin-Siris syndrome

Disease Ontology (DO):
DOID:0070057 - Coffin-Siris syndrome 9