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Links from OMIM

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HEPHL1
(A355T)
Single nucleotide variant
(missense variant)
Pili torti-developmental delay-neurological abnormalities syndrome
GPathogenic
ATP7A
(G1373fs +1 more)
Deletion
(frameshift variant +1 more)
Cutis laxa, X-linked
GConflicting classifications of pathogenicity