GlyCosmos Diseases

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

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 2251 - 2275 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:0080576
  • spondyloepimetaphyseal dysplasia, Genevieve-type
Mus musculus (house mouse)
DOID:3407
  • carotid artery disease
  • Aliases:
    • disorder of carotid artery
Mus musculus (house mouse)
DOID:3407
  • carotid artery disease
  • Aliases:
    • disorder of carotid artery
Rattus norvegicus (Norway rat)
DOID:2367
  • neuroaxonal dystrophy
Rattus norvegicus (Norway rat)
DOID:0112319
  • Kanzaki disease
  • Aliases:
    • NAGA deficiency type 2
    • adult-onset alpha-N-acetylgalactosaminidase deficiency
    • alpha-N-acetylgalactosaminidase deficiency type 2
Rattus norvegicus (Norway rat)
DOID:14499
  • Fabry disease
  • Aliases:
    • Alpha-galactosidase A deficiency
    • Angiokeratoma Corporis Diffusum
    • Fabry Disease, Cardiac Variant
    • Fabry's disease
    • alpha galactosidase deficiency
    • deficiency of melibiase
Rattus norvegicus (Norway rat)
DOID:0112318
  • Schindler disease type 1
  • Aliases:
    • NAGA deficiency type 1
    • alpha-N-acetylgalactosaminidase deficiency type 1
Rattus norvegicus (Norway rat)
DOID:479
  • angiokeratoma
  • Aliases:
    • Angiokeratoma of skin
    • Cutaneous Angiokeratoma
    • skin angiokeratoma
Rattus norvegicus (Norway rat)
DOID:0112318
  • Schindler disease type 1
  • Aliases:
    • NAGA deficiency type 1
    • alpha-N-acetylgalactosaminidase deficiency type 1
Mus musculus (house mouse)
DOID:479
  • angiokeratoma
  • Aliases:
    • Angiokeratoma of skin
    • Cutaneous Angiokeratoma
    • skin angiokeratoma
Mus musculus (house mouse)
DOID:2367
  • neuroaxonal dystrophy
Mus musculus (house mouse)
DOID:0112319
  • Kanzaki disease
  • Aliases:
    • NAGA deficiency type 2
    • adult-onset alpha-N-acetylgalactosaminidase deficiency
    • alpha-N-acetylgalactosaminidase deficiency type 2
Mus musculus (house mouse)
DOID:14499
  • Fabry disease
  • Aliases:
    • Alpha-galactosidase A deficiency
    • Angiokeratoma Corporis Diffusum
    • Fabry Disease, Cardiac Variant
    • Fabry's disease
    • alpha galactosidase deficiency
    • deficiency of melibiase
Mus musculus (house mouse)
DOID:0090059
  • enhanced S-cone syndrome
Homo sapiens (human)
DOID:0110871
  • congenital stationary night blindness 2A
  • Aliases:
    • congenital stationary night blindness 2A X-linked
Homo sapiens (human)
DOID:0110008
  • achromatopsia 3
  • Aliases:
    • ACHM1
    • ACHM3
    • Pingelapese blindness
    • RMCH1
    • rod monochromacy 1
    • rod monochromatism 1
Homo sapiens (human)
DOID:0110865
  • congenital stationary night blindness 1B
  • Aliases:
    • CSNB1B
    • autosomal recessive complete congenital stationary night blindness
    • congenital stationary night blindness 1B autosomal recessive
Homo sapiens (human)
DOID:4692
  • endophthalmitis
Homo sapiens (human)
DOID:0080411
  • familial adenomatous polyposis 3
Homo sapiens (human)
DOID:0080325
  • tuberous sclerosis 2
Homo sapiens (human)
DOID:0060308
  • autosomal recessive intellectual developmental disorder
  • Aliases:
    • autosomal recessive mental retardation
    • autosomal recessive non-syndromic mental retardation
Homo sapiens (human)
DOID:0080411
  • familial adenomatous polyposis 3
Saccharomyces cerevisiae S288C
DOID:10792
  • chronic maxillary sinusitis
  • Aliases:
    • chronic antritis
Homo sapiens (human)
DOID:12904
  • mucocele of salivary gland
  • Aliases:
    • Mucous retention cyst of salivary gland
    • Ranula
    • Salivary Cyst
    • Salivary gland mucocele
Homo sapiens (human)
DOID:0111582
  • hereditary arterial and articular multiple calcification syndrome
  • Aliases:
    • CALJA
    • arterial calcification and distal joint calcification
    • arterial calcification due to CD73 deficiency
    • arterial calcification due to deficiency of CD73
    • calcification of joints and arteries
Homo sapiens (human)

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Last updated: August 19, 2024