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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ELF4
(N223I)
Single nucleotide variant
(missense variant)
Autoinflammatory syndrome, familial, X-linked, Behcet-like 2
GUncertain significance
ELF4
(V242M)
Single nucleotide variant
(missense variant)
Autoinflammatory syndrome, familial, X-linked, Behcet-like 2
GUncertain significance
ELF4
Single nucleotide variant
(missense variant)
Autoinflammatory syndrome, familial, X-linked, Behcet-like 2
GPathogenic
ELF4
(A339fs)
Deletion
(frameshift variant)
Autoinflammatory syndrome, familial, X-linked, Behcet-like 2
GPathogenic
ELF4
(W251S)
Single nucleotide variant
(missense variant)
Autoinflammatory syndrome, familial, X-linked, Behcet-like 2
GPathogenic
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