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MIM:214150 - CEREBROOCULOFACIOSKELETAL SYNDROME 1; COFS1
Xenbase Genes: ercc6, ercc5
Human Disease Resource: MIM
MONDO:0008926 - COFS syndrome |
MONDO:0008955 - cerebrooculofacioskeletal syndrome 1 |
MONDO:0016006 - Cockayne syndrome |
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MONDO:0008926 - COFS syndrome |
MONDO:0008955 - cerebrooculofacioskeletal syndrome 1 |
MONDO:0016006 - Cockayne syndrome |