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Nume Neural Tube Defects, Folate-Sensitive
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Boli A-Z Abdominal Wall Defect Aging Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Anauxetic Dysplasia 1 Anencephaly Aniridia 1 Anorexia Nervosa 1 Arachnoid Cysts Arachnoiditis Arthrochalasia Ehlers-Danlos Syndrome Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Bowen-Conradi Syndrome Cervical Spina Bifida Aperta Cervical Spina Bifida Cystica Cervicothoracic Spina Bifida Aperta Cervicothoracic Spina Bifida Cystica Chiari Malformation Choroiditis Chromosomal Triplication Ciliopathy Cleft Lip Corpus Callosum, Agenesis of, with Abnormal Genitalia Cranioectodermal Dysplasia 1 Craniorachischisis Craniosynostosis Diabetes Mellitus Diastematomyelia Diprosopus Down Syndrome Dysostosis Encephalocele Exencephaly Fetal Alcohol Syndrome Gastroschisis Gestational Diabetes Glucose Intolerance Helicobacter Pylori Infection Hemangioma-Thrombocytopenia Syndrome Hepatic Adenomas, Familial Heterotaxy Holoprosencephaly Homocysteinemia Homocystinuria Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Hydrocephalus Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperglycemia Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypogonadotropic Hypogonadism 1 with or Without Anosmia Hypopituitarism Iniencephaly Ischemia Kabuki Syndrome 1 Klippel-Feil Syndrome Lateral Meningocele Syndrome Lenz-Majewski Hyperostotic Dwarfism Lipomyelomeningocele Lumbosacral Spina Bifida Aperta Lumbosacral Spina Bifida Cystica Malaria Mature Teratoma Megaloblastic Anemia Meningocele Methylmalonic Aciduria and Homocystinuria, Cblc Type Methylmalonic Aciduria and Homocystinuria Type Cble Methylmalonic Aciduria and Homocystinuria Type Cblg Methylmalonic Aciduria, Cblb Type Mosaic Variegated Aneuploidy Syndrome 1 Myelocystocele Myelomeningocele Neural Tube Defects Neurodegeneration with Brain Iron Accumulation 2a Neuronitis Neuropathy Nondisjunction Occipital Encephalocele Omphalocele Orofacial Cleft Ovarian Cyst Persistent Idiopathic Facial Pain Placental Abruption Placental Choriocarcinoma Polydactyly Preaxial Hallucal Polydactyly Propionic Acidemia Schizophrenia Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sirenomelia Spina Bifida Occulta Spinal Arachnoiditis Split Foot Split Hand Syringohydromyelia Teratoma Tethered Cord Syndrome Thoracolumbosacral Spina Bifida Aperta Thoracolumbosacral Spina Bifida Cystica Thrombophilia Thyroiditis Total Spina Bifida Aperta Total Spina Bifida Cystica Transcobalamin Ii Deficiency Treacher Collins Syndrome 1 Upper Thoracic Spina Bifida Aperta Upper Thoracic Spina Bifida Cystica Urinary Tract Obstruction Vacterl Association Van Der Woude Syndrome 1 Vascular Disease Vater/vacterl Association Vitamin B12 Deficiency Vitamin Metabolic Disorder Waardenburg Syndrome, Type 1 Waardenburg Syndrome, Type 3