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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Microcephaly, epilepsy, and diabetes syndrome
Microcephaly, epilepsy, and diabetes syndrome 2
rare
Identifiers
MONDO:0025690
OMIM:619278
Causal genes
YIPF5
Part of
Microcephaly, epilepsy, and diabetes syndrome
Also known as
MEDS2
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