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Summary Literature (0)
MIM:616817 - MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2; MSSGM2


Xenbase Genes: ppp1r15b

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014785 - microcephaly, short stature, and impaired glucose metabolism 2
MONDO:0018320 - primary microcephaly-mild intellectual disability-young-onset diabetes syndrome