Informaţii despre

Nume Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type
Pagina Web www.malacards.org
Clasificare globală Malacards Boli genetice; Boli rare
Clasificare anatomică Malacards Boli neuronale; Boli psihice

Vezi şi

Boli A-Z 12q14 Microdeletion Syndrome Acromegaly Adenocarcinoma Adenoma Aging Agoraphobia Alacrima, Achalasia, and Mental Retardation Syndrome Alagille Syndrome 1 Aland Island Eye Disease Alcohol Dependence Allergic Asthma Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alpha-Thalassemia/mental Retardation Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arteries, Anomalies of Arthrochalasia Ehlers-Danlos Syndrome Asthma Atrial Fibrillation Autism X-Linked 2 Autoimmune Lymphoproliferative Syndrome Autoimmune Myocarditis Beta-Adrenergic Stimulation, Response to 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 Bone Fracture Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brain Cancer Brain Injury Breast Cancer Breast Disease Burns Cannabis Dependence Cervicitis Clear Cell Renal Cell Carcinoma Coffin-Siris Syndrome 1 Colitis Colon Adenocarcinoma Corneal Neovascularization Dementia Dental Caries Diencephalic Syndrome Endotheliitis Epithelial Recurrent Erosion Dystrophy Extraosseous Osteosarcoma Frontotemporal Dementia Galactose Epimerase Deficiency Gastrinoma Hemangioma Hemifacial Hyperplasia Hepatic Adenomas, Familial Hepatic Lipase Deficiency Hepatitis Hepatitis C Hepatitis C Virus Herpes Simplex Human Coronavirus Sensitivity Human T-Cell Leukemia Virus Type 1 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoactive Sexual Desire Disorder Hypothalamic Hamartomas Hypotonia Idiopathic Scoliosis Infertility Influenza Keloids Lactic Acidosis Laron Syndrome Leukemia Leukoencephalopathy, Hereditary Diffuse, with Spheroids Leukotriene C4 Synthase Deficiency Lipoid Proteinosis of Urbach and Wiethe Liver Disease Logopenic Progressive Aphasia Lung Cancer Lupus Erythematosus Lutheran Suppressor, X-Linked Lymphoid Interstitial Pneumonia Malaria Malignant Hyperthermia Migraine with or Without Aura 1 Mungan Syndrome Muscular Atrophy Myocardial Infarction Myocarditis Myopia Osteoporosis Pancreatic Cancer Pancreatic Ductal Carcinoma Pancreatitis Panic Disorder Paraganglioma Pectus Carinatum Periodic Limb Movement Disorder Peritonitis Pneumonia Prostate Cancer Prostatitis Resting Heart Rate, Variation in Retinitis Retinoschisis 1, X-Linked, Juvenile Reye Syndrome Rhabdomyosarcoma Richards-Rundle Syndrome Robinow Syndrome, Autosomal Recessive Salt and Pepper Developmental Regression Syndrome Scoliosis Sialadenitis Silver-Russell Syndrome Silver-Russell Syndrome Due to Maternal Uniparental Disomy of Chromosome 7 Skin Hemangioma Smith-Magenis Syndrome Spasticity Spinal Cord Injury Spinal Muscular Atrophy Spondylolisthesis Stiff-Person Syndrome Swine Influenza Syndromic X-Linked Intellectual Disability Syndromic X-Linked Intellectual Disability Snyder Type Systemic Lupus Erythematosus T-Cell Leukemia Traumatic Brain Injury Treacher Collins Syndrome 1 Trigeminal Neuralgia Ulcerative Colitis