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MIM:614249 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 18, WITH OR WITHOUT EPILEPSY; MRT18
Xenbase Genes: med23
Human Disease Resource: MIM
MONDO:0013651 - intellectual disability, autosomal recessive 18 |
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability |
DOID:0060308 - autosomal recessive intellectual developmental disorder |
DOID:0081190 - autosomal recessive intellectual developmental disorder 18 |