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Summary Literature (3)
OMIM:194190 - WOLF-HIRSCHHORN SYNDROME; WHS


Xenbase Genes: nsd2, cplx1, ctbp1, letm1, fgfrl1, nelfa

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008684 - Wolf-Hirschhorn syndrome

Disease Ontology (DO):
DOID:0050460 - Wolf-Hirschhorn syndrome