Additional Disease Briefs

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Rare Disease Database Reports Additional Rare Disease Briefs
ALG6-congenital disorder of glycosylation 1C

Also known as: ALG6 congenital disorder of glycosylation, ALG6-CDG, ALG6-CDG (CDG-Ic), ALG6-CDG1C, ALG6-congenital disorder of glycosylation 1C, CDG 1C, CDG Ic, CDG syndrome type Ic, CDG-Ic, CDG1C, CDGIc, CDGS5 (formerly), carbohydrate deficient glycoprotein syndrome type Ic, carbohydrate-deficient glycoprotein syndrome type 1C, carbohydrate-deficient glycoprotein syndrome, type 1 with deficient glycosylation of dolichol-linked oligosaccharide (formerly), carbohydrate-deficient glycoprotein syndrome, type I, with deficient glycosylation of dolichol-linked oligosaccharide, carbohydrate-deficient glycoprotein syndrome, type I, with deficient glycosylation of dolichol-linked oligosaccharide, formerly, carbohydrate-deficient glycoprotein syndrome, type V, carbohydrate-deficient glycoprotein syndrome, type V (formerly), carbohydrate-deficient glycoprotein syndrome, type V, formerly, congenital disorder of glycosylation caused by mutation in ALG6, congenital disorder of glycosylation type 1C, congenital disorder of glycosylation type Ic, congenital disorder of glycosylation, type Ic, glucosyltransferase 1 deficiency

ALG8-congenital disorder of glycosylation

Also known as: ALG8-CDG, ALG8-CDG (CDG-Ih), ALG8-congenital disorder of glycosylation, CDG 1H, CDG Ih, CDG syndrome type Ih, CDG-Ih, CDG1H, carbohydrate deficient glycoprotein syndrome type Ih, congenital disorder of glycosylation type 1h, congenital disorder of glycosylation type Ih, congenital disorder of glycosylation, type Ih, glucosyltransferase 2 deficiency

ALG9-associated autosomal dominant polycystic kidney disease

Also known as: ALG9 autosomal dominant polycystic kidney disease, ALG9 related autosomal dominant polycystic kidney disease, ALG9-associated ADPKD, ALG9-associated autosomal dominant polycystic kidney disease, Autosomal Dominant Polycystic Kidney Disease - ALG9, autosomal dominant polycystic kidney disease caused by mutation in ALG9

ALG9-congenital disorder of glycosylation

Also known as: ALG9-CDG, ALG9-CDG (CDG-IL), ALG9-congenital disorder of glycosylation, CDG 1L, CDG IL, CDG syndrome type IL, CDG-IL, CDG1L, carbohydrate deficient glycoprotein syndrome type 1L, carbohydrate deficient glycoprotein syndrome type IL, congenital disorder of glycosylation type 1L, congenital disorder of glycosylation type IL, congenital disorder of glycosylation, type IL, mannosyltransferase 7-9 deficiency

ALK-positive large B-cell lymphoma

Also known as: ALK+ LBCL, ALK+ large B-cell lymphoma, ALK-DLBCL, ALK-positive large B-cell lymphoma, diffuse large B-cell lymphoma with expression of full-length ALK, diffuse large B-cell lymphoma with expression of full-length anaplastic lymphoma kinase

alkaline ceramidase 3 deficiency

Also known as: ACER3-related early childhood-onset progressive leukodystrophy, PLDECO, leukodystrophy due to alkaline ceramidase 3 deficiency, leukodystrophy, progressive, early childhood-onset

Alkhurma hemorrhagic fever

Also known as: Alkhumra hemorrhagic fever virus caused disease or disorder, Alkhumra hemorrhagic fever virus disease or disorder, Alkhumra hemorrhagic fever virus infectious diseaseAlkhumra hemorrhagic fever virus caused disease or disorder, Alkhumra hemorrhagic fever virus disease or disorder, Alkhumra hemorrhagic fever virus infectious disease

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