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 July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 1126 - 1150 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:12347
  • osteogenesis imperfecta
  • Aliases:
    • Lobstein's syndrome
    • Osteopsathyrosis
    • Vrolik's disease
    • brittle bone disease
Homo sapiens (human)
DOID:10608
  • celiac disease
  • Aliases:
    • celiac sprue
    • coeliac disease
    • idiopathic steatorrhea
Homo sapiens (human)
DOID:299
  • adenocarcinoma
Homo sapiens (human)
DOID:0110011
  • advanced sleep phase syndrome 1
  • Aliases:
    • FASPS1
    • familial advanced sleep phase syndrome 1
Homo sapiens (human)
DOID:0110258
  • cataract 10 multiple types
  • Aliases:
    • CTRCT10
Homo sapiens (human)
DOID:0111401
  • congenital dyserythropoietic anemia type II
  • Aliases:
    • CDA II
    • CDA type 2
    • CDA type II
    • CDAN2
    • Congenital dyserythropoietic anaemia type 2
    • Congenital dyserythropoietic anemia type 2
    • Hereditary erythroblastic multinuclearity with a positive acidified-serum test (hempas)
    • SEC23B-CDG
    • congenital dyserythropoietic anaemia type II
Homo sapiens (human)
DOID:0060673
  • Peters anomaly
Homo sapiens (human)
DOID:11211
  • buphthalmos
  • Aliases:
    • primary congenital glaucoma 3A
    • simple buphthalmos
Homo sapiens (human)
DOID:0112233
  • lissencephaly 8
  • Aliases:
    • LIS8
Homo sapiens (human)
DOID:0060179
  • Renpenning syndrome
  • Aliases:
    • Golabi-Ito-Hall syndrome
    • Sutherland-Haan X-linked mental retardation syndrome
    • X-linked intellectual disability due to PQBP1 mutations
    • X-linked intellectual disability, Renpenning type
    • X-linked mental retardation Renpenning type
    • X-linked mental retardation with spastic diplegia
    • syndromic X-linked mental retardation 8
Homo sapiens (human)
DOID:13664
  • post-vaccinal encephalitis
  • Aliases:
    • Encephalitis following immunization procedures
    • Postvaccinal encephalomyelitis
Homo sapiens (human)
DOID:0050564
  • autosomal dominant nonsyndromic deafness
  • Aliases:
    • autosomal dominant deafness
Homo sapiens (human)
DOID:0110231
  • cataract 1 multiple types
  • Aliases:
    • CTRCT1
    • Duffy linked cataract
    • cataract 1, multiple types, with or without microcornea
Homo sapiens (human)
DOID:0111135
  • congenital generalized lipodystrophy type 1
  • Aliases:
    • Berardinelli-Seip Congenital Lipodystrophy, Type 1
    • Brunzell syndrome AGPAT2-related
Homo sapiens (human)
DOID:0110206
  • Charcot-Marie-Tooth disease dominant intermediate F
  • Aliases:
    • CMTDIF
    • autosomal dominant intermediate Charcot-Marie-Tooth disease type F
Homo sapiens (human)
DOID:0050459
  • hyperphosphatemia
Homo sapiens (human)
DOID:0110849
  • xeroderma pigmentosum group G
  • Aliases:
    • XP group G
    • XP7
    • XPG
    • xeroderma pigmentosum VII
Homo sapiens (human)
DOID:5453
  • pulmonary venoocclusive disease
  • Aliases:
    • pulmonary veno-occlusive disease
Homo sapiens (human)
DOID:3078
  • anaplastic astrocytoma
  • Aliases:
    • grade III Astrocytic tumor
    • grade III astrocytoma
Homo sapiens (human)
DOID:0050795
  • cone dystrophy
  • Aliases:
    • retinal cone dystrophy
Homo sapiens (human)
DOID:0060473
  • Kabuki syndrome
  • Aliases:
    • KMS
    • Kabuki make up syndrome
    • Niikawa-Kuroki syndrome
Homo sapiens (human)
DOID:8501
  • fundus dystrophy
  • Aliases:
    • Retinal Dystrophy
Homo sapiens (human)
DOID:10352
  • breast fibroadenosis
  • Aliases:
    • Fibroadenosis - breast
    • Fibroadenosis of breast
Homo sapiens (human)
DOID:7165
  • subacute thyroiditis
  • Aliases:
    • De Quervain's thyroiditis
    • Giant-cell thyroiditis
    • Granulomatous thyroiditis
    • Subacute Granulomatous Thyroiditis
Homo sapiens (human)
DOID:0050458
  • juvenile myelomonocytic leukemia
Homo sapiens (human)

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Last updated: August 19, 2024