Informaţii despre

Nume Congenital Disorder of Glycosylation, Type in
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10 Other disorders of glycoprotein metabolism
Clasificare anatomică Malacards Boli ale urechii; Boli cardiovasculare; Boli de piele; Boli de sânge; Boli endocrine; Boli gastrointestinale; Boli hepatice; Boli musculare; Boli nefrologice (ale rinichilor); Boli neuronale; Boli osoase; Boli psihice
Boli din aceeaşi familie Congenital Disorder of Glycosylation, Type I/iix; Congenital Disorder of Glycosylation, Type Ia; Congenital Disorder of Glycosylation, Type Ib; Congenital Disorder of Glycosylation, Type Ic; Congenital Disorder of Glycosylation, Type Id; Congenital Disorder of Glycosylation, Type Ie; Congenital Disorder of Glycosylation, Type if; Congenital Disorder of Glycosylation, Type Ig; Congenital Disorder of Glycosylation, Type Ih; Congenital Disorder of Glycosylation, Type Ii; Congenital Disorder of Glycosylation, Type Iia; Congenital Disorder of Glycosylation, Type Iib; Congenital Disorder of Glycosylation, Type Iic; Congenital Disorder of Glycosylation, Type Iid; Congenital Disorder of Glycosylation, Type Iif; Congenital Disorder of Glycosylation, Type Iig; Congenital Disorder of Glycosylation, Type Iih; Congenital Disorder of Glycosylation, Type Iii; Congenital Disorder of Glycosylation, Type Iij; Congenital Disorder of Glycosylation, Type Iik; Congenital Disorder of Glycosylation, Type Iil; Congenital Disorder of Glycosylation, Type Iim; Congenital Disorder of Glycosylation, Type Iin; Congenital Disorder of Glycosylation, Type Iio; Congenital Disorder of Glycosylation, Type Iip; Congenital Disorder of Glycosylation, Type Iiq; Congenital Disorder of Glycosylation, Type Ij; Congenital Disorder of Glycosylation, Type Ik; Congenital Disorder of Glycosylation, Type Il; Congenital Disorder of Glycosylation, Type Im; Congenital Disorder of Glycosylation, Type Io; Congenital Disorder of Glycosylation, Type Ip; Congenital Disorder of Glycosylation, Type Iq; Congenital Disorder of Glycosylation, Type Ir; Congenital Disorder of Glycosylation, Type It; Congenital Disorder of Glycosylation, Type Iu; Congenital Disorder of Glycosylation, Type Iw; Congenital Disorder of Glycosylation, Type Ix; Congenital Disorder of Glycosylation, Type Iy

Vezi şi

Boli A-Z 3-Hydroxyacyl-Coa Dehydrogenase Deficiency Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Aspartylglucosaminuria Ataxia and Polyneuropathy, Adult-Onset Ataxia-Oculomotor Apraxia 3 Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, I System Brain Small Vessel Disease with or Without Ocular Anomalies Camurati-Engelmann Disease Carbohydrate Metabolic Disorder Cardiac Rupture Cerebral Hemorrhage Cerebritis Cervical Dystonia Cervicitis Congenital Disorder of Glycosylation, Type Ia Congenital Disorder of Glycosylation, Type Ib Congenital Disorder of Glycosylation, Type Ic Congenital Disorder of Glycosylation, Type Id Congenital Disorder of Glycosylation, Type Ie Congenital Disorder of Glycosylation, Type if Congenital Disorder of Glycosylation, Type Ig Congenital Disorder of Glycosylation, Type Ih Congenital Disorder of Glycosylation, Type Ii Congenital Disorder of Glycosylation, Type Iia Congenital Disorder of Glycosylation, Type Iib Congenital Disorder of Glycosylation, Type Iic Congenital Disorder of Glycosylation, Type Iid Congenital Disorder of Glycosylation, Type Iih Congenital Disorder of Glycosylation, Type I/iix Congenital Disorder of Glycosylation, Type Ij Congenital Disorder of Glycosylation, Type Ik Congenital Disorder of Glycosylation, Type Il Congenital Disorder of Glycosylation, Type Im Congenital Disorder of Glycosylation, Type It Congenital Disorder of Glycosylation, Type Ix Congenital Disorders of N-Linked Glycosylation and Multiple Pathway Congenital Myasthenic Syndromes with Glycosylation Defect Cutis Laxa Diarrhea Dilated Cardiomyopathy Dystonia Encephalopathy Epileptic Encephalopathy, Early Infantile, 36 Evans' Syndrome Extrinsic Allergic Alveolitis Fetal Akinesia Deformation Sequence Fructose Intolerance, Hereditary Galactosemia Glucosephosphate Dehydrogenase Deficiency Glycogen Storage Disease Hemihyperplasia, Isolated Hepatic Adenomas, Familial Hepatitis Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hyperinsulinemic Hypoglycemia Hypertrophic Cardiomyopathy Hypoglycemia Hypotonia Ichthyosis, Congenital, Autosomal Recessive 11 Ichthyosis Prematurity Syndrome Immune Hydrops Fetalis Immune Suppression Immunoglobulin E Concentration, Serum Laryngeal Cleft Lissencephaly 1 Liver Disease Malignant Migrating Partial Seizures of Infancy Melancholia Meningitis Mucopolysaccharidosis, Type Ii Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3 Muscular Dystrophy Muscular Dystrophy, Congenital, Lmna-Related Myopathy Myopathy, Congenital Pericardial Effusion Peters-Plus Syndrome Pmm2-Congenital Disorder of Glycosylation Polycystic Liver Disease Protein-Losing Enteropathy Retinitis Skeletal Dysplasias Stt3a-Cdg and Stt3b-Cdg Tenosynovial Giant Cell Tumor Thrombocytopenia Thrombophilia Wrinkles