|
OMIM:613192 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 13; MRT13
Xenbase Genes: trappc9, trappc9.2
Human Disease Resource: OMIM
MONDO:0013173 - intellectual disability, autosomal recessive 13 |
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability |
DOID:0050889 - non-syndromic intellectual disability |