INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary

Literature (0)

MIM:615502 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21

Xenbase Genes: ctcf

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014213 - CTCF-related neurodevelopmental disorder

MONDO:0014213 - CTCF-related neurodevelopmental disorder

Disease Ontology (DO):

DOID:0070051 - autosomal dominant intellectual developmental disorder 21

DOID:0070051 - autosomal dominant intellectual developmental disorder 21