Congenital Disorders of N-Linked Glycosylation and Multiple Pathway

Nume		Congenital Disorders of N-Linked Glycosylation and Multiple Pathway
Pagina Web		www.malacards.org

Boli A-Z		Alcohol Abuse Aniridia 1 Anorexia Nervosa 1 Autosomal Recessive Disease Blood Group--Ahonen Blood Group, I System Brachydactyly Cataract Cerebellar Hypoplasia Congenital Disorder of Glycosylation, Type Ib Congenital Disorder of Glycosylation, Type Id Congenital Disorder of Glycosylation, Type Ie Congenital Disorder of Glycosylation, Type Io Dysostosis Epileptic Encephalopathy, Early Infantile, 36 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I Hepatitis Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hyperinsulinemic Hypoglycemia Hypoglycemia Laryngeal Cleft Olivopontocerebellar Atrophy Parkinson Disease 15, Autosomal Recessive Early-Onset Pmm2-Congenital Disorder of Glycosylation Thyroiditis