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MIM:616033 - MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1; MSSGM1
Xenbase Genes: trmt10a
Human Disease Resource: OMIM
MONDO:0000208 - microcephaly, short stature, and impaired glucose metabolism 1 |
MONDO:0018320 - primary microcephaly-mild intellectual disability-young-onset diabetes syndrome |