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Links from OMIM

Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FRMD5
(P200fs +3 more)
Deletion
(frameshift variant +1 more)
Neurodevelopmental disorder with eye movement abnormalities and ataxia
GUncertain significance
FRMD5
(L143V +2 more)
Single nucleotide variant
(missense variant +2 more)
Neurodevelopmental disorder with eye movement abnormalities and ataxia
GUncertain significance
FRMD5
(G124D +3 more)
Single nucleotide variant
(missense variant +1 more)
Neurodevelopmental disorder with eye movement abnormalities and ataxia
GUncertain significance
FRMD5
(S117N +3 more)
Single nucleotide variant
(missense variant +1 more)
Neurodevelopmental disorder with eye movement abnormalities and ataxia
GLikely pathogenic
FRMD5
(K60N +2 more)
Single nucleotide variant
(missense variant +2 more)
Neurodevelopmental disorder with eye movement abnormalities and ataxia
GUncertain significance
FRMD5
(S354P +3 more)
Single nucleotide variant
(missense variant +1 more)
Neurodevelopmental disorder with eye movement abnormalities and ataxia
GPathogenic
FRMD5
(S351G +3 more)
Single nucleotide variant
(missense variant +1 more)
Neurodevelopmental disorder with eye movement abnormalities and ataxia
GPathogenic
FRMD5
(Y312C +1 more)
Single nucleotide variant
(missense variant +2 more)
Neurodevelopmental delay
GUncertain significance
FRMD5
(S115R +3 more)
Single nucleotide variant
(missense variant +1 more)
Neurodevelopmental disorder with eye movement abnormalities and ataxia
+1 more
GConflicting classifications of pathogenicity
FRMD5
(C118R +3 more)
Single nucleotide variant
(missense variant +1 more)
See cases
GUncertain significance
FRMD5
(S117R +3 more)
Single nucleotide variant
(missense variant +1 more)
See cases
GUncertain significance
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