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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DHDDS
(R37C)
Single nucleotide variant
(missense variant +1 more)
Developmental delay and seizures with or without movement abnormalities
+2 more
GPathogenic
DHDDS
(K42E)
Single nucleotide variant
(missense variant +1 more)
Retinitis pigmentosa 59
+3 more
GPathogenic
DHDDS
(R205Q +3 more)
Single nucleotide variant
(missense variant)
Retinitis pigmentosa 59
+2 more
GPathogenic
DHDDS
Single nucleotide variant
(splice acceptor variant)
Retinitis pigmentosa 59
+1 more
GLikely pathogenic
DHDDS
(F203L +3 more)
Single nucleotide variant
(missense variant)
Developmental delay and seizures with or without movement abnormalities
GUncertain significance
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