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MIM:611091 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 5; MRT5
Xenbase Genes: nsun2
Human Disease Resource: MIM
| MONDO:0012613 - intellectual disability, autosomal recessive 5 |
| MONDO:0019502 - autosomal recessive non-syndromic intellectual disability |
| DOID:0060308 - autosomal recessive intellectual developmental disorder |
| DOID:0081181 - autosomal recessive intellectual developmental disorder 5 |
