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Summary Literature (0)
MIM:610756 - CEREBROOCULOFACIOSKELETAL SYNDROME 2; COFS2

Xenbase Genes: ercc2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008926 - COFS syndrome
MONDO:0012553 - cerebrooculofacioskeletal syndrome 2
MONDO:0016006 - Cockayne syndrome

Disease Ontology (DO):
DOID:0080912 - cerebrooculofacioskeletal syndrome 2