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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
UROD
(Y311C)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
UROD
(P62L)
Single nucleotide variant
(missense variant +1 more)
not provided
GPathogenic
UROD
(R292G)
Single nucleotide variant
(missense variant +1 more)
Hepatoerythropoietic porphyria
GPathogenic
UROD
(E167K)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
UROD
(G281E)
Single nucleotide variant
(missense variant +1 more)
not provided
GPathogenic
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