Cornelia de Lange syndrome 1 (Q63226394)
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Cornelia de Lange syndrome that has material basis in heterozygous mutation in the NIPBL gene, which encodes a component of the cohesin complex, on chromosome 5p13
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Cornelia de Lange syndrome 1 |
Cornelia de Lange syndrome that has material basis in heterozygous mutation in the NIPBL gene, which encodes a component of the cohesin complex, on chromosome 5p13 |
Statements
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Identifiers
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