Genes & Conditions

Here's what we test for

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Select a product gene list
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Picture Parenting gene list

Picture Parenting looks for 30 genetic conditions that you may be able to pass on to your children, even if you don't show symptoms yourself.
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Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency - ACADM Expand Icon
Canavan disease - ASPA Expand Icon
Citrullinemia - ASS1 Expand Icon
Bloom Syndrome - BLM Expand Icon
Cystic Fibrosis - CFTR Expand Icon
Neuronal ceroid lipofuscinosis, CLN3-related - CLN3 Expand Icon
Smith-Lemli-Opitz syndrome - DHCR7 Expand Icon
Duchenne Muscular Dystrophy - DMD Expand Icon
Fanconi anemia group C - FANCC Expand Icon
Tyrosinemia, type 1 - FAH Expand Icon
Fragile X syndrome - FMR1 Expand Icon
Glycogen storage disease, type 1a - G6PC Expand Icon
Pompe disease - GAA Expand Icon
Galactosemia - GALT Expand Icon
Gaucher disease - GBA Expand Icon
Alpha thalassemia - HBA1 / HBA2 Expand Icon
Mucopolysaccharidosis, type I (Hurler syndrome) - IDUA Expand Icon
Phenylalanine Hydroxylase deficiency (Phenylketonuria) - PAH Expand Icon
Isovaleric Acidemia - IVD Expand Icon
Zellweger syndrome, PEX1-related - PEX1 Expand Icon
Rhizomelic chondrodysplasia punctata, type 1 - PEX7 Expand Icon
Polycystic kidney disease, PKHD1-related - PKHD1 Expand Icon
Congenital disorder of glycosylation type 1a - PMM2 Expand Icon
Spinal muscular atrophy - SMN1 Expand Icon
Niemann-Pick disease, type A/B - SMPD1 Expand Icon
Familial Dysautonomia - IKBKAP Expand Icon
Methylmalonic aciduria and homocystinuria, cblC type - MMACHC Expand Icon
Sickle cell disease - HBB Expand Icon
Tay-Sachs disease - HEXA Expand Icon
Beta thalassemia - HBB Expand Icon