Genomics England
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Panels
Genes and Entities
SLC35A3
solute carrier family 35 member A3
OMIM:
605632
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Panel
Mode of inheritance
Details
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Arthrogryposis
R-numbers:
R83
Signed-off version 8.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Arthrogryposis, impaired intellectual development, and seizures, OMIM:615553