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Microcephaly, short stature, and impaired glucose metabolism 2
rareAny microcephaly, short stature, and impaired glucose metabolism in which the cause of the disease is a mutation in the PPP1R15B gene.
- Identifiers
- MONDO:0014785 OMIM:616817
- Causal genes
- PPP1R15B
- Also known as
- 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 · MSSGM2 · PPP1R15B microcephaly, short stature, and impaired glucose metabolism
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