RS121909152 PEX7
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What This Variant Does
"[OMIM:?]
Associated Conditions
Rhizomelic chondrodysplasia punctata type 1
Peroxisome biogenesis disorder 9B
Rhizomelic chondrodysplasia punctata
Inborn genetic diseases
Rhizomelic chondrodysplasia punctata type 1
Peroxisome biogenesis disorder 9B
Rhizomelic chondrodysplasia punctata
Inborn genetic diseases
Other Variants in PEX7