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Cornelia de Lange syndrome 1
Summary
- Definition
- A 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.
- Super Class
- Cornelia de Lange syndrome autosomal dominant disease
External Links
- Disease Ontology
- DOID:0080505
- Mondo Disease Ontology
- OMIM
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O95271 | Poly [ADP-ribose] polymerase tankyrase-1 | |
| P51689 | Arylsulfatase D | |
| Q96FL9 | Polypeptide N-acetylgalactosaminyltransferase 14 | |
| Q9UQE7 | Structural maintenance of chromosomes protein 3 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000545 | Myopia |
| HP:0000574 | Thick eyebrow |
| HP:0000639 | Nystagmus |
| HP:0000664 | Synophrys |
| HP:0000667 | Phthisis bulbi |
| HP:0000684 | Delayed eruption of teeth |
| HP:0000687 | Widely spaced teeth |
| HP:0000717 | Autism |
| HP:0000722 | Compulsive behaviors |
| HP:0000739 | Anxiety |
