GRIN2B-related complex neurodevelopmental disorder
MONDO:0700350A complex neurodevelopmental disorder caused by a variation in the GRIN2B gene
1 clinical trial for this condition and its sub-types.
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Broader categories
Disease
(717)
Nervous system disorder
(243)
Hereditary disease
(188)
Neurodevelopmental disorder
(154)
Human disease
(15)
Hereditary neurological disease
(6)
Complex neurodevelopmental disorder
(3)
Disease of genetic or genomic mechanism
(2)
GRIN-related complex neurodevelopmental disorder
(2)
Disease by body system or component
(0)