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MIM:614499 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY; MRT34
Xenbase Genes: cradd.2, cradd
Human Disease Resource: MIM
MONDO:0013785 - intellectual disability, autosomal recessive 34 |
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability |
DOID:0060308 - autosomal recessive intellectual developmental disorder |