Informaţii despre

Nume Prader-Willi Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Congenital malformation syndromes predominantly associated with short stature
Clasificare anatomică Malacards Boli ale sistemului reproducator; Boli endocrine; Boli neuronale
Boli din aceeaşi familie Prader-Willi Syndrome Due to Imprinting Mutation; Prader-Willi Syndrome Due to Maternal Uniparental Disomy of Chromosome 15; Prader-Willi Syndrome Due to Paternal 15q11q13 Deletion; Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1; Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 2; Prader-Willi Syndrome Due to Translocation; Prader-Willi-Like Syndrome Due to a Point Mutation

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Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 47, Xxy Abdominal Obesity-Metabolic Syndrome 1 Ablepharon-Macrostomia Syndrome Acanthosis Nigricans Acid-Labile Subunit Deficiency Acidophil Adenoma Acquired Generalized Lipodystrophy Acquired Metabolic Disease Acromegaly Adrenal Gland Hyperfunction Aging Albinism Albinism, Oculocutaneous, Type Ii Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Angelman Syndrome Angelman Syndrome Due to Imprinting Defect in 15q11-Q13 Angelman Syndrome Due to Maternal 15q11q13 Deletion Aniridia 1 Anorexia Nervosa 1 Anovulation Apnea, Obstructive Sleep Apparent Mineralocorticoid Excess Aromatase Deficiency Arteries, Anomalies of Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Asperger Syndrome Autism Autism 6 Autism Spectrum Disorder Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blount's Disease 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 Bulimia Nervosa 1 Bulimia Nervosa 2 Cardiac Tamponade Central Precocious Puberty Cerebellar Atrophy, Developmental Delay, and Seizures Cerebellar Hypoplasia Cerebritis Charge Syndrome Childhood Electroclinical Syndrome Chromophobe Adenoma Chromosomal Disease Chromosomal Triplication Chromosome 15q11-Q13 Duplication Syndrome Chromosome 15q Deletion Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency Cohen Syndrome Compartment Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Ectropion Uveae Congenital Hepatic Fibrosis Congenital Hypothyroidism Constipation Cranioectodermal Dysplasia 1 Craniopharyngioma Cryptorchidism, Unilateral or Bilateral Dementia Diabetes Mellitus Dilated Cardiomyopathy Distal Arthrogryposis Down Syndrome Dumping Syndrome Eating Disorder Ectropion Empty Sella Syndrome Endocrine Pancreas Disease Endotheliitis Epilepsy Factor Xi Deficiency Fanconi Anemia, Complementation Group E Fasting Hypoglycemia Fatty Liver Disease Fetal Alcohol Syndrome Fetal Macrosomia Fragile X Syndrome Functioning Pituitary Adenoma Gastric Dilatation Gastrointestinal System Disease Gestational Diabetes Glomerulonephritis Glucose Intolerance Glucose Metabolism Disease Gonadal Disease Growth Control, Y-Chromosome Influenced Growth Hormone Deficiency Hepatic Adenomas, Familial Hepatitis Hyperandrogenism Hyperglycemia Hyperinsulinism Hyperpituitarism Hyperproinsulinemia Hyperprolactinemia Hypersomnia Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoadrenalism Hypoglycemic Coma Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypomelanosis of Ito Hypopituitarism Hypothalamic Disease Hypothyroidism, Congenital, Nongoitrous, 4 Hypotonia Idiopathic Central Precocious Puberty Idiopathic Recurrent Pericarditis Infertility Insulin-Like Growth Factor I Intermittent Explosive Disorder Isodicentric 15 Isodicentric Chromosome 15 Syndrome Isolated Growth Hormone Deficiency Isolated Growth Hormone Deficiency, Type Ib Juvenile Hereditary Hemochromatosis Kleine-Levin Hibernation Syndrome Laron Syndrome Learning Disability Leptin, Serum Level of, Quantitative Trait Locus 1 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Lupus Erythematosus Lutheran Suppressor, X-Linked Lymphedema Membranoproliferative Glomerulonephritis Meninges Hemangiopericytoma Metabolic Acidosis Microcephaly, Epilepsy, and Diabetes Syndrome Moebius Syndrome Morbid Obesity Mosaic Trisomy 15 Mosaic Variegated Aneuploidy Syndrome 1 Mucolipidosis Iv Multiple Symmetrical Lipomatosis Muscular Dystrophy Neurodegeneration with Brain Iron Accumulation 2a Neuronitis Nonalcoholic Steatohepatitis Norrie Disease Nutritional Deficiency Disease Obesity, Hyperphagia, and Developmental Delay Obesity-Hypoventilation Syndrome Obsessive-Compulsive Disorder Ocular Albinism Oculocutaneous Albinism Ovarian Disease Overnutrition Pachyonychia Congenita 1 Pancreas Disease Pancreatic Cholera Pancreatitis Panniculitis Partington X-Linked Mental Retardation Syndrome Periodontal Disease Periodontitis Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities Pituitary Adenoma 1, Multiple Types Pituitary Apoplexy Pituitary-Dependent Cushing's Disease Pituitary Gland Disease Pituitary Hormone Deficiency, Combined, 2 Pituitary Infarct Polycystic Ovary Syndrome Polydactyly, Postaxial, with Progressive Myopia Polyhydramnios Postorgasmic Illness Syndrome Prader-Willi Syndrome Due to Imprinting Mutation Prader-Willi Syndrome Due to Maternal Uniparental Disomy of Chromosome 15 Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 1 Prader-Willi Syndrome Due to Paternal Deletion of 15q11q13 Type 2 Prader-Willi Syndrome Due to Translocation Precocious Puberty Prediabetes Syndrome Premature Ovarian Failure 1 Schaaf-Yang Syndrome Scoliosis Secondary Adrenal Insufficiency Seizure Disorder Sheehan Syndrome Short Bowel Syndrome Silver-Russell Syndrome Skin/hair/eye Pigmentation, Variation in, 1 Sleep Apnea Sleep Disorder Slipped Capital Femoral Epiphysis Smith-Magenis Syndrome Sotos Syndrome 1 Spinal Cord Injury Stereotypic Movement Disorder Systemic Lupus Erythematosus Tay-Sachs Disease Temple Syndrome Testicular Disease Thrombosis Thyroiditis Transsexualism Transsexuality Trimethylaminuria Turner Syndrome Type 1 Diabetes Mellitus 15 Uremia Woodhouse-Sakati Syndrome