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
Displaying all 4 entries
Gene ID Gene Symbol Description Source
414 ARSD arylsulfatase D
8658 TNKS tankyrase
9126 SMC3 structural maintenance of chromosomes 3
79623 GALNT14 polypeptide N-acetylgalactosaminyltransferase 14
The Human Phenotype Ontology
Displaying entries 51 - 60 of 99 in total
HPO ID HPO Term
HP:0001387 Joint stiffness
HP:0001508 Failure to thrive
HP:0001511 Intrauterine growth retardation
HP:0001557 Prenatal movement abnormality
HP:0001622 Premature birth
HP:0001629 Ventricular septal defect
HP:0001631 Atrial septal defect
HP:0001770 Toe syndactyly
HP:0001773 Short foot
HP:0001883 Talipes
Displaying 1 entry
Gene ID Gene Symbol Description
9126 SMC3 structural maintenance of chromosomes 3

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024