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MIM:614231 - MICROCEPHALY, EPILEPSY, AND DIABETES SYNDROME 1; MEDS1
Xenbase Genes: ier3ip1
Human Disease Resource: MIM
MONDO:0013647 - obsolete primary microcephaly-epilepsy-permanent neonatal diabetes syndrome |
MONDO:0031481 - microcephaly, epilepsy, and diabetes syndrome 1 |