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Summary Literature (0)
MIM:300749 - INTELLECTUAL DEVELOPMENTAL DISORDER WITH MICROCEPHALY AND PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH

Xenbase Genes: cask

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010417 - syndromic X-linked intellectual disability Najm type

Disease Ontology (DO):
DOID:0060807 - syndromic X-linked intellectual disability Najm type