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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HPDL, LOC129930439
(M1I)
Single nucleotide variant
(missense variant +1 more)
Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities
+1 more
GPathogenic
GAD1
Single nucleotide variant
(intron variant)
Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities
GConflicting classifications of pathogenicity