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Agenesis of Corpus Callosum

Birth defect that results in a partial or complete absence of the CORPUS CALLOSUM. It may be isolated or a part of a syndrome (e.g., AICARDI'S SYNDROME; ACROCALLOSAL SYNDROME; ANDERMANN SYNDROME; and HOLOPROSENCEPHALY). Clinical manifestations include neuromotor skill impairment and INTELLECTUAL DISABILITY of variable severity.

Subtype terms (4)

More specific conditions that are subtypes of Agenesis of Corpus Callosum in the MeSH hierarchy.

ICD-10 crosswalk