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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
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Mendelian neurodevelopmental disorder
Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities
Identifiers
MONDO:0060664
OMIM:617913
Causal genes
GEMIN4
Part of
Mendelian neurodevelopmental disorder
Also known as
NEDMCR
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