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Summary Literature (0)
MIM:617125 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 56; MRT56

Xenbase Genes: zc3h14

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014930 - perivascular space
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability