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Summary Literature (0)
MIM:210720 - MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2

Xenbase Genes: pcnt

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008872 - microcephalic osteodysplastic primordial dwarfism type II

Disease Ontology (DO):
DOID:0060609 - microcephalic osteodysplastic primordial dwarfism type II