The Cornelia de Lange syndrome (CDLS) is a multisystem malformation syndrome recognized primarily on the basis of characteristic facial dysmorphism, ...

Cornelia de Lange syndrome is a clinically heterogeneous developmental disorder characterized by malformations affecting multiple systems.

Cornelia de Lange syndrome is a multisystem developmental disorder characterized by distinctive facial dysmorphism, pre- and postnatal growth failure, ...

Cornelia de Lange syndrome is a clinically heterogeneous developmental disorder characterized by malformations affecting multiple systems. Affected individuals ...

A number sign (#) is used with this entry because Cornelia de Lange syndrome-4 with or without midline brain defects (CDLS4) is caused by heterozygous ...

Cornelia de Lange syndrome (CDLS) is a genetically heterogeneous developmental disorder characterized by malformations affecting multiple systems.

Cornelia de Lange syndrome is a clinically heterogeneous developmental disorder characterized by malformations affecting multiple systems. Affected individuals ...

Online Mendelian Inheritance in Man (OMIM) is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and ...

122470, CORNELIA DE LANGE SYNDROME 1; CDLS1. 300040, STRUCTURAL MAINTENANCE OF CHROMOSOMES 1A; SMC1A. 300269, HISTONE DEACETYLASE 8; HDAC8.

CORNELIA DE LANGE SYNDROME 5; CDLS5 · Height. - Short stature (family H) [SNOMEDCT: 237836003, 422065006, 237837007] [ICD10CM: E34. · Weight. - Truncal obesity ( ...