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Summary Literature (0)
MIM:136000 - ADERMATOGLYPHIA; ADERM

Xenbase Genes: smarcad1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007619 - isolated congenital adermatoglyphia

Disease Ontology (DO):
DOID:0111357 - adermatoglyphia