You are using an outdated browser. Please upgrade your browser to improve your experience.

corpus callosum, agenesis of

Disease Summary
Associated Targets (3)
Tbio

3


Explore Associated Targets
Mondo Description A congenital abnormality characterized by the complete absence of the corpus callosum. It may be an isolated abnormality or associated with other central nervous system abnormalities or syndromes. Clinical manifestations vary. In cases of isolated corpus callosum agenesis, symptoms may be absent or minimal. In cases that are associated with other central nervous system abnormalities or syndromes, symptoms include developmental delays, motor coordination difficulties, and vision impairment.
Mondo Term and Equivalent IDs
MONDO:0009022:  corpus callosum, agenesis of
GARD:0001535: 
MESH:D061085: 
NCIT:C98905: 
SCTID:5102002: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found