Microcephaly, short stature, and impaired glucose metabolism 2

MONDO:0014785

Any microcephaly, short stature, and impaired glucose metabolism in which the cause of the disease is a mutation in the PPP1R15B gene.

Also known as: MSSGM2, PPP1R15B microcephaly, short stature, and impaired glucose metabolism, microcephaly, short stature, and impaired glucose metabolism 2, microcephaly, short stature, and impaired glucose metabolism 2; MSSGM2, microcephaly, short stature, and impaired glucose metabolism caused by mutation in PPP1R15B, microcephaly, short stature, and impaired glucose metabolism type 2

0 clinical trials for this condition and its sub-types, 0 tagged with Microcephaly, short stature, and impaired glucose metabolism 2 itself.

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Including sub-types (0) Tagged with Microcephaly, short stature, and impaired glucose metabolism 2 (0)

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