INTELLECTUAL DEVELOPMENTAL DISORDER WITH MICROCEPHALY AND WITH OR WITHOUT OCULAR MALFORMATIONS OR HYPOGONADOTROPIC HYPOGONADISM; IDDMOH

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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: OMIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014376 - intellectual disability, autosomal dominant 27
MONDO:0015452 - Coffin-Siris syndrome

MONDO:0014376 - intellectual disability, autosomal dominant 27

MONDO:0015452 - Coffin-Siris syndrome

Disease Ontology (DO):

DOID:0070057 - Coffin-Siris syndrome 9

DOID:0070057 - Coffin-Siris syndrome 9