Informaţii despre

Nume Neural Tube Defects
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificari ICD10 Unspecified spina bifida with hydrocephalus
Clasificare anatomică Malacards Boli neuronale

Vezi şi

Boli A-Z Abdominal Wall Defect Acromelic Frontonasal Dysostosis Acute Lymphoblastic Leukemia, Childhood Acute Respiratory Distress Syndrome Adenocarcinoma Adie Pupil Adult Acute Lymphocytic Leukemia Aging Agnosia Albinism-Deafness Syndrome Allergic Hypersensitivity Disease Alobar Holoprosencephaly Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha-Fetoprotein Deficiency Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amenorrhea Anauxetic Dysplasia 1 Andersen Cardiodysrhythmic Periodic Paralysis Androgen Insensitivity Syndrome, Mild Anencephaly Anencephaly and Spina Bifida X-Linked Angel-Shaped Phalangoepiphyseal Dysplasia Aniridia 1 Anorexia Nervosa 1 Anuria Anus, Imperforate Arachnoid Cysts Arachnoiditis Arterial Tortuosity Syndrome Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Ataxia Neuropathy Spectrum Auditory Agnosia Autism Axenfeld-Rieger Syndrome Back Pain Bacterial Meningitis Bacteriuria Bladder Adenocarcinoma Bladder Cancer Bladder Squamous Cell Carcinoma Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 1 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 Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bowen-Conradi Syndrome Breast Cancer Breast Secretory Carcinoma Brooke-Spiegler Syndrome Cat Eye Syndrome Caudal Duplication Anomaly Cerebral Palsy Cerebritis Cerebrospinal Fluid Leak Cervical Spina Bifida Aperta Cervical Spina Bifida Cystica Cervicitis Cervicothoracic Spina Bifida Aperta Cervicothoracic Spina Bifida Cystica Charles Bonnet Syndrome Chiari Malformation Choroiditis Chromosomal Triplication Ciliopathy Cleft Lip Cleft Lip/palate Clubfoot Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly Collecting Duct Carcinoma Cone-Rod Dystrophy 2 Conotruncal Heart Malformations Constipation Corpus Callosum, Agenesis of, with Abnormal Genitalia Cranial Meningocele Cranioectodermal Dysplasia 1 Craniorachischisis Craniosynostosis Crouzon Syndrome with Acanthosis Nigricans Decubitus Ulcer Detrusor Sphincter Dyssynergia Diabetes Mellitus Diaphragmatic Hernia, Congenital Diastematomyelia Digeorge Syndrome Diprosopus Down Syndrome Dysostosis Elephantiasis Encephalocele Endotheliitis Epilepsy Exencephaly Fecal Incontinence Fetal Alcohol Syndrome Fruit Allergy Gastroschisis Gestational Diabetes Glioblastoma Glucose Intolerance Gonadal Dysgenesis Headache Helicobacter Pylori Infection Hemangioma-Thrombocytopenia Syndrome Hemochromatosis, Neonatal Hepatic Adenomas, Familial Heterotaxy Holoprosencephaly Holoprosencephaly 5 Homocysteinemia Homocystinuria Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Horseshoe Kidney Hydrocephalus Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius Hydrocephalus, Nonsyndromic, Autosomal Recessive 2 Hydromyelia Hydronephrosis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperacusis Hyperglycemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertrichosis Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypogonadotropic Hypogonadism 1 with or Without Anosmia Hypopituitarism Idiopathic Scoliosis Immunoglobulin E Concentration, Serum Iniencephaly Ischemia Juvenile Rheumatoid Arthritis Kabuki Syndrome 1 Kasznica Carlson Coppedge Syndrome Klippel-Feil Syndrome Lateral Meningocele Syndrome Latex Allergy Learning Disability Lenz-Majewski Hyperostotic Dwarfism Linear Scleroderma Lipomyelomeningocele Lissencephaly 1 Lumbosacral Spina Bifida Aperta Lumbosacral Spina Bifida Cystica Lymphedema Macular Dystrophy, Retinal, 1, North Carolina Type Malaria Mature Teratoma Megaloblastic Anemia Megaloblastic Anemia Due to Dihydrofolate Reductase Deficiency Meningitis Meningocele Methotrexate Toxicity or Dose Selection 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 Muscular Dystrophy Myelocystocele Myelomeningocele Neural Tube Defects, Folate-Sensitive Neurodegeneration with Brain Iron Accumulation 2a Neurofibroma Neurofibromatosis, Type Iv, of Riccardi Neurogenic Bladder Neurogenic Bowel Neuronitis Neuropathy Nipples, Supernumerary Occipital Encephalocele Oeis Complex Omphalocele Orofacial Cleft Osteochondroma Ovarian Cyst Paine Syndrome Paraplegia Pediatric Osteosarcoma Pentalogy of Cantrell Persistent Idiopathic Facial Pain Pilonidal Sinus Pituitary Hormone Deficiency, Combined, 2 Placental Choriocarcinoma Polydactyly Porencephaly Preaxial Hallucal Polydactyly Propionic Acidemia Rheumatoid Arthritis Richards-Rundle Syndrome Robinow Syndrome, Autosomal Recessive Sacral Defect with Anterior Meningocele Sacral Meningocele Conotruncal Heart Defects Sacrococcygeal Teratoma Schisis Association Schizophrenia Scoliosis Sebastian Syndrome Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Shwachman-Diamond Syndrome Sirenomelia Situs Inversus Spastic Ataxia, Charlevoix-Saguenay Type Spina Bifida Aperta Spina Bifida Occulta Spinal Arachnoiditis Spinal Cord Injury Split Foot Split Hand Split Spinal Cord Malformation Spondylocostal Dysostosis 1, Autosomal Recessive Spondylolisthesis Spondylolysis Spondyloocular Syndrome Spondylosis Squamous Cell Carcinoma Status Epilepticus Strabismus Syringohydromyelia Syringomyelia Talipes Equinovarus Teratoma Testicular Cancer Tethered Cord Syndrome Tetraploidy Thiamine Metabolism Dysfunction Syndrome 2 Thoracoabdominal 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 Triploidy Tuberous Sclerosis 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 Ventricular Septal Defect Vesicoureteral Reflux 1 Vitamin B12 Deficiency Vitamin Metabolic Disorder Waardenburg Syndrome, Type 1 Waardenburg Syndrome, Type 3