Genes & Conditions

Here's what we test for

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.
Want a downloadable PDF?
Have It
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