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Summary Literature (0)
MIM:617506 - NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2

Xenbase Genes: ppp1cb

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054588 - DPYSL5

Disease Ontology (DO):
DOID:0080693 - Noonan syndrome-like disorder with loose anagen hair 2