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Summary Literature (0)
MIM:300886 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 32; MRXS32

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010473 - X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome

Disease Ontology (DO):
DOID:0060828 - X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome