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Summary Literature (0)
MIM:614202 - RAFIQ SYNDROME; RAFQS

Xenbase Genes: man1b1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013624 - Rafiq syndrome
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability

Disease Ontology (DO):
DOID:0050889 - non-syndromic intellectual disability
DOID:0081097 - Rafiq syndrome