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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 hypotonia, poor growth, dysmorphic facies, and agammaglobulinemia
Identifiers
MONDO:0976131
OMIM:621068
Causal genes
SEL1L
Part of
Mendelian neurodevelopmental disorder
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