Informaţii despre

Nume Velocardiofacial Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Di George syndrome
Clasificare anatomică Malacards Boli ale urechii; Boli cardiovasculare; Boli de sânge; Boli endocrine; Boli nefrologice (ale rinichilor); Boli neuronale

Vezi şi

Boli A-Z Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Apraxia Arthritis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Attention Deficit-Hyperactivity Disorder Autism Bernard-Soulier Syndrome Blepharocheilodontic Syndrome 1 Blood Group--Ahonen Blood Group, I System Blood Platelet Disease Brown Syndrome Cardiofaciocutaneous Syndrome 1 Cat Eye Syndrome Cayler Cardiofacial Syndrome Cervicitis Chiari Malformation Childhood-Onset Schizophrenia Chromosomal Deletion Syndrome Chromosomal Disease Chromosome 22q11.2 Duplication Syndrome Chronic Granulomatous Disease Conotruncal Heart Malformations Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Dementia Digeorge Syndrome Digeorge Syndrome/velocardiofacial Syndrome Complex 2 Distal Arthrogryposis Down Syndrome Dysphasia, Familial Developmental Ear Malformation Epilepsy Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome Fanconi Anemia, Complementation Group E Fragile X Syndrome Genitopatellar Syndrome Graves' Disease Heart Septal Defect Hepatic Adenomas, Familial Hyperprolinemia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hyperthyroidism Hypoparathyroidism Hypotonia Influenza Inherited Blood Coagulation Disease Juvenile Rheumatoid Arthritis L-2-Hydroxyglutaric Aciduria Learning Disability Leukemia Monosomy 22 Myeloid Leukemia Neurodegeneration with Brain Iron Accumulation 2a Opitz-Gbbb Syndrome Palatopharyngeal Incompetence Personality Disorder Pharyngitis Phelan-Mcdermid Syndrome Phobia, Specific Polykaryocytosis Inducer Portal Hypertension Rheumatoid Arthritis Schizophrenia Scoliosis Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Specific Language Impairment Speech Disorder Tetralogy of Fallot Thrombocytopenia Tooth Agenesis Transposition of the Great Arteries Turner Syndrome Uveitis