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Boli A-Z Acquired Thrombocytopenia Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Anencephaly Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Arthropathy 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 Cerebral Palsy Cerebritis Cerebrospinal Fluid Leak Cerebrovascular Disease Cervical Spina Bifida Aperta Cervical Spina Bifida Cystica Cervicitis Cervicomedullary Junction Neoplasm Cervicothoracic Spina Bifida Aperta Cervicothoracic Spina Bifida Cystica Charles Bonnet Syndrome Chiari Malformation Chiari Malformation Type Ii Choroiditis Clubfoot Clubfoot, Congenital, with or Without Deficiency of Long Bones and/or Mirror-Image Polydactyly Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cone-Rod Dystrophy 2 Constipation Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia Craniorachischisis Diaphragmatic Hernia, Congenital Diastematomyelia Digeorge Syndrome Dysostosis Elephantiasis Encephalocele Epilepsy Fecal Incontinence Focal Dermal Hypoplasia Glycine N-Methyltransferase Deficiency Growth Hormone Deficiency Hepatic Adenomas, Familial Hip Subluxation Homocysteinemia Homocystinuria Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity Hydrocephalus Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius Hydromyelia Hyperreflexia Internuclear Ophthalmoplegia Ischemic Neuropathy Klippel-Feil Syndrome Latex Allergy Learning Disability Lens Subluxation Lipomatosis Lipomyelomeningocele Lumbosacral Lipoma Lumbosacral Spina Bifida Aperta Lumbosacral Spina Bifida Cystica Megaloblastic Anemia Meningitis Meningocele Metabolic Acidosis Methane Production Methylmalonic Aciduria and Homocystinuria, Cblc Type Methylmalonic Aciduria and Homocystinuria Type Cble Methylmalonic Aciduria and Homocystinuria Type Cblg Methylmalonic Aciduria, Cblb Type Multiple Sclerosis Muscular Dystrophy Myoclonus Nephrotic Syndrome Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neurenteric Cyst Neurodegeneration with Brain Iron Accumulation 2a Neurogenic Bladder Neurogenic Bowel Neuronitis Nondisjunction Oligoastrocytoma Optic Nerve Hypoplasia, Bilateral Osteomyelitis Parkinson Disease 15, Autosomal Recessive Early-Onset Peritonitis Peters-Plus Syndrome Placental Choriocarcinoma Poland Syndrome Precocious Puberty Scoliosis Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Sleep Disorder Spastic Ataxia, Charlevoix-Saguenay Type Spasticity Spina Bifida Aperta Spina Bifida Occulta Spinal Cord Injury Spondylitis Spondylolysis Spondyloocular Syndrome Steel Syndrome Strabismus Syringohydromyelia Syringomyelia Talipes Equinovarus Teratoma Tethered Cord Syndrome Tethered Spinal Cord Syndrome Thoracolumbosacral Spina Bifida Aperta Thoracolumbosacral Spina Bifida Cystica Thrombosis Tonsillitis Tooth Agenesis Total Spina Bifida Aperta Total Spina Bifida Cystica Transcobalamin Ii Deficiency Undifferentiated Pleomorphic Sarcoma Upper Thoracic Spina Bifida Aperta Upper Thoracic Spina Bifida Cystica Urethritis Vitamin B12 Deficiency Vitamin Metabolic Disorder Waardenburg Syndrome, Type 3