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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 8951 - 8975 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0110444
  • dilated cardiomyopathy 1X
  • Aliases:
    • CMD1X
    • dilated cardiomyopathy with mild or no proximal muscle weakness
Xenopus laevis (African clawed frog)
DOID:1849
  • cannabis dependence
Saccharomyces cerevisiae S288C
DOID:14503
  • neuronal ceroid lipofuscinosis
  • Aliases:
    • hereditary ceroid lipofuscinosis
Danio rerio (zebrafish)
DOID:1307
  • dementia
Homo sapiens (human)
DOID:0080746
  • Sweet syndrome
  • Aliases:
    • Acute Febrile Neutrophilic Dermatosis
    • Sweet's syndrome
Homo sapiens (human)
DOID:0090125
  • brain small vessel disease 1
  • Aliases:
    • BSVD1
    • COL4A1-related brain small vessel disease with hemorrhage
    • COL4A1-related familial vascular leukoencephalopathy
    • COL4A1-related retinal arteriolar tortuosity-infantile hemiparesis-autosomal dominant leukoencephalopathy syndrome
    • autosomal dominant retinal arteriolar tortuosity, infantile hemiparesis, and leukencephalopathy
    • brain small vessel disease with Axenfeld-Riegar anomaly
    • brain small vessel disease with hemorrhage
    • brain small vessel disease with or without ocular anomalies
    • infantile hemiparesis
    • leukoencephalopathy with Axenfeld-Riegar anomaly
Homo sapiens (human)
DOID:0112266
  • nephrotic syndrome type 23
  • Aliases:
    • NPHS23
Mus musculus (house mouse)
DOID:374
  • nutrition disease
  • Aliases:
    • Nutritional disorder
Homo sapiens (human)
DOID:0080573
  • congenital disorder of glycosylation Ix
  • Aliases:
    • congenital disorder of glycosylation 1x
Rattus norvegicus (Norway rat)
DOID:7148
  • rheumatoid arthritis
  • Aliases:
    • Arthritis or polyarthritis, rheumatic
    • atrophic Arthritis
Saccharomyces cerevisiae S288C
DOID:0081441
  • Nicolaides-Baraitser syndrome
  • Aliases:
    • Intellectual disability-sparse hair-brachydactyly syndrome
    • SPARSE HAIR-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME
Homo sapiens (human)
DOID:0050970
  • spinocerebellar ataxia type 19/22
Drosophila melanogaster (fruit fly)
DOID:0110861
  • autosomal recessive polycystic kidney disease
  • Aliases:
    • Arpkd
    • Pkhd1
    • Polycystic Kidney Disease, Infantile, Type I
    • Polycystic Kidney and Hepatic Disease 1
Mus musculus (house mouse)
DOID:0060193
  • amyotrophic lateral sclerosis type 1
  • Aliases:
    • ALS1
    • amyotrophic lateral sclerosis 1
Homo sapiens (human)
DOID:4531
  • mucoepidermoid carcinoma
  • Aliases:
    • MEC
Mus musculus (house mouse)
DOID:0050474
  • Netherton syndrome
Mus musculus (house mouse)
DOID:0080384
  • nephrotic syndrome type 6
Homo sapiens (human)
DOID:13976
  • peptic esophagitis
  • Aliases:
    • Peptic reflux disease
    • Reflux oesophagitis
    • reflux esophagitis
Drosophila melanogaster (fruit fly)
DOID:0112198
  • spondyloepimetaphyseal dysplasia with joint laxity type 1
  • Aliases:
    • SEMDJL1
    • spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures
Rattus norvegicus (Norway rat)
DOID:0060853
  • Potocki-Lupski syndrome
  • Aliases:
    • 17p11.2 microduplication syndrome
    • chromosome 17p11.2 duplication syndrome
    • trisomy 17p11.2
Mus musculus (house mouse)
DOID:4928
  • intrahepatic cholangiocarcinoma
  • Aliases:
    • Intrahepatic bile duct carcinoma
    • peripheral Cholangiocarcinoma
Rattus norvegicus (Norway rat)
DOID:0060747
  • Duane-radial ray syndrome
  • Aliases:
    • DR syndrome
    • Duane anomaly with radial ray abnormalities and deafness
    • Okihiro syndrome
    • acrorenocular syndrome
Mus musculus (house mouse)
DOID:4001
  • ovarian carcinoma
Drosophila melanogaster (fruit fly)
DOID:2750
  • glycogen storage disease IV
  • Aliases:
    • Amylopectinosis
    • Branching-transferase deficiency glycogenosis
    • Glycogen storage disease 4
    • Glycogen storage disease, type IV
    • brancher deficiency glycogenosis
    • deficiency of 1,4-alpha-glucan branching enzyme
Saccharomyces cerevisiae S288C
DOID:0111096
  • Fanconi anemia complementation group O
  • Aliases:
    • FANCO
Homo sapiens (human)
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Last updated: December 9, 2024