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Summary Literature (0)
MIM:213000 - CEREBELLAR HYPOPLASIA/ATROPHY, EPILEPSY, AND GLOBAL DEVELOPMENTAL DELAY; CHEGDD

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008939 - isolated cerebellar hypoplasia/agenesis
MONDO:0016392 - mastoid lymph node

Disease Ontology (DO):
DOID:0070339 - cerebellar hyplasia/atrophy, epilepsy, and global developmental delay