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Links from OMIM

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FBXL3
(R149*)
Single nucleotide variant
(nonsense)
Intellectual disability, short stature, facial anomalies, and joint dislocations
GPathogenic
FIG4
(I41T)
Single nucleotide variant
(missense variant)
Bilateral parasagittal parieto-occipital polymicrogyria
+7 more
GPathogenic/Likely pathogenic