INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 41; MRT41

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:615637 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 41; MRT41

Xenbase Genes: kptn

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014289 - macrocephaly-developmental delay syndrome

MONDO:0014289 - macrocephaly-developmental delay syndrome

Disease Ontology (DO):

DOID:0060308 - autosomal recessive intellectual developmental disorder
DOID:0081206 - autosomal recessive intellectual developmental disorder 41

DOID:0060308 - autosomal recessive intellectual developmental disorder

DOID:0081206 - autosomal recessive intellectual developmental disorder 41