Steroid Inherited Metabolic Disorder,Myopathy, Centronuclear, 4,Classic Congenital Adrenal Hyperplasia Due To 21-Hydroxylase Deficiency,Disorder Of Sexual Development,Kohler'S Disease,Familial Glucocorticoid Deficiency,Synostosis,Cortisone Reductase Deficiency,Radioulnar Synostosis,Craniosynostosis,Cytochrome P450 Oxidoreductase Deficiency,Premature Menopause,Amenorrhea,Disordered Steroidogenesis Due To Cytochrome P450 Oxidoreductase Deficiency,46,Xy Sex Reversal,Corneal Dystrophy, Posterior Polymorphous, 1,Crouzon Syndrome,Adrenal Insufficiency, Congenital, With 46,Xy Sex Reversal, Partial Or Complete,Asperger Syndrome,Antley-Bixler Syndrome,Odontochondrodysplasia,Persistent Mullerian Duct Syndrome,Humeroradial Synostosis,Lipoid Congenital Adrenal Hyperplasia,Antley-Bixler Syndrome With Genital Anomalies And Disordered Steroidogenesis,Antley-Bixler Syndrome Without Genital Anomalies Or Disordered Steroidogenesis

Ventricular Septal Defect,Heart Disease,Physical Disorder,Vascular Disease,Amino Acid Metabolic Disorder,Homocystinuria,Nondisjunction,Methylmalonic Acidemia Without Homocystinuria,Cleft Lip,Fallopian Tube Disease,Placental Abruption,Cleft Lip/Palate,Ophthalmia Neonatorum,Bacterial Conjunctivitis,Male Infertility,Neural Tube Defects, Folate-Sensitive,Rectal Disease,Disorders Of Intracellular Cobalamin Metabolism,Methotrexate Toxicity,Migraine With Aura,Megaloblastic Anemia,Urethritis,Urethral Syndrome,Cardia Cancer,Anus Disease,Homocysteinemia,Methylmalonic Acidemia,Homocystinuria-Megaloblastic Anemia, Cble Complementation Type,Neural Tube Defects,Orofacial Cleft,Vitamin Metabolic Disorder,Vitamin B12 Deficiency,Methylmalonic Aciduria And Homocystinuria Type Cble,Methylmalonic Aciduria And Homocystinuria Type Cblg,Down Syndrome,Autism Spectrum Disorder,Lipoprotein Quantitative Trait Locus,Anencephaly,Myelomeningocele,Chromosomal Duplication Syndrome,Marfan Syndrome,Phenylketonuria