Silver-Russell Syndrome

Informaţii despre

Nume		Silver-Russell 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
Boli din aceeaşi familie		Silver-Russell Syndrome Due to a Point Mutation; Silver-Russell Syndrome Due to an Imprinting Defect of 11p15; Silver-Russell Syndrome Due to Maternal Uniparental Disomy of Chromosome 11; Silver-Russell Syndrome Due to Maternal Uniparental Disomy of Chromosome 7

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Boli A-Z		12q14 Microdeletion Syndrome Acid-Labile Subunit Deficiency Acromegaly Adult Mesoblastic Nephroma Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Angiomatosis Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Arts Syndrome Astrocytoma Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autoimmune Lymphoproliferative Syndrome Beckwith-Wiedemann Syndrome Beckwith-Wiedemann Syndrome Due to Imprinting Defect of 11p15 Benign Mesenchymoma Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Choriocarcinoma Chromosomal Triplication Chromosome 11p Duplication Coffin-Siris Syndrome 1 Congenital Anomalies of Kidney and Urinary Tract 2 Conjunctivitis Craniopharyngioma Curry-Jones Syndrome Cystic Fibrosis Diabetes Mellitus, Transient Neonatal, 1 Diencephalic Syndrome Diffuse Idiopathic Skeletal Hyperostosis Down Syndrome Dwarfism Dystonia Fanconi Anemia, Complementation Group E Fetal Macrosomia Growth Hormone Deficiency Hemihyperplasia, Isolated Hepatoblastoma Hydatidiform Mole, Recurrent, 1 Hyperinsulinism Hypoglycemia Hypopituitarism Ichthyosis, Congenital, Autosomal Recessive 1 Idiopathic Central Precocious Puberty Immunoglobulin E Concentration, Serum Insulin-Like Growth Factor I Isolated Growth Hormone Deficiency, Type Ia Isolated Growth Hormone Deficiency, Type Ib Juvenile Pilocytic Astrocytoma Kagami-Ogata Syndrome Laron Syndrome Learning Disability Mayer-Rokitansky-Kuster-Hauser Syndrome Meninges Hemangiopericytoma Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type Mesocardia Mosaic Trisomy 7 Myoclonus Nutritional Deficiency Disease Persistent Fetal Circulation Syndrome Pilocytic Astrocytoma Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities Pituitary Adenoma 1, Multiple Types Renal Tubular Acidosis Rigid Spine Muscular Dystrophy 1 Ring Chromosome 15 Ring Chromosome 7 Robinow-Sorauf Syndrome Salivary Gland Adenoma, Pleomorphic Secondary Adrenal Insufficiency Sensorineural Hearing Loss Silver-Russell Syndrome Due to 11p15 Microduplication Silver-Russell Syndrome Due to an Imprinting Defect of 11p15 Silver-Russell Syndrome Due to a Point Mutation Silver-Russell Syndrome Due to Maternal Uniparental Disomy of Chromosome 11 Silver-Russell Syndrome Due to Maternal Uniparental Disomy of Chromosome 7 Slipped Capital Femoral Epiphysis Spastic Paraplegia 17, Autosomal Dominant Spondyloocular Syndrome Syndromic X-Linked Intellectual Disability Snyder Type Temple Syndrome Tetraamelia Syndrome, Autosomal Recessive Three M Syndrome 1 Turner Syndrome Umbilical Hernia Uniparental Disomy of Chromosome 11 Wilms Tumor 5