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 3601 - 3625 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:0060610
  • megacystis-microcolon-intestinal hypoperistalsis syndrome
  • Aliases:
    • Berdon syndrome
    • Megacystis microcolon intestinal hypoperistalsis syndrome
    • megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH
    • visceral myopathy
Homo sapiens (human)
DOID:0111128
  • focal segmental glomerulosclerosis 1
  • Aliases:
    • FSGS1
Homo sapiens (human)
DOID:0111134
  • focal segmental glomerulosclerosis 9
  • Aliases:
    • FSGS9
Homo sapiens (human)
DOID:0080572
  • congenital disorder of glycosylation Iw
  • Aliases:
    • congenital disorder of glycosylation 1w
Mus musculus (house mouse)
DOID:701
  • dentin dysplasia
  • Aliases:
    • Dentinal dysplasia
Homo sapiens (human)
DOID:0110058
  • amelogenesis imperfecta type 1E
  • Aliases:
    • AIH1
    • X-linked amelogenesis imperfecta 1
    • X-linked amelogenesis imperfecta hypoplastic/hypomaturation 1
    • amelogenesis imperfecta hypomaturationtype with snow-capped teeth
    • amelogenesis imperfecta type IE
Homo sapiens (human)
DOID:2187
  • amelogenesis imperfecta
Homo sapiens (human)
DOID:0110066
  • amelogenesis imperfecta type 1G
  • Aliases:
    • AI1G
    • AIGFS
    • ERS
    • amelogenesis imperfecta and gingival fibromatosis syndrome
    • amelogenesis imperfecta hypoplastic with nephrocalcinosis
    • amelogenesis imperfecta type IG
    • enamel-renal syndrome
    • enamel-renal-gingival syndrome
Homo sapiens (human)
DOID:0110055
  • amelogenesis imperfecta type 3A
  • Aliases:
    • ADHCAI
    • amelogenesis imperfecta hypomineralization type
    • amelogenesis imperfecta type III
    • autosomal dominant amelogenesis imperfecta hypocalcification type
Homo sapiens (human)
DOID:0110059
  • X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2
  • Aliases:
    • AIH3
    • amelogenesis imperfecta type IE X-linked 2
    • amelogenesis imperfecta 3 hypoplastic type
Homo sapiens (human)
DOID:0110063
  • amelogenesis imperfecta hypomaturation type 2A5
  • Aliases:
    • AI2A5
    • amelogenesis imperfecta hypomaturation type IIA5
    • amelogenesis imperfecta type IIA5
Homo sapiens (human)
DOID:0110057
  • amelogenesis imperfecta type 2A1
  • Aliases:
    • AI2A1
    • amelogenesis imperfecta pigmented hypomaturation type 1
    • amelogenesis imperfecta type IIA1
Homo sapiens (human)
DOID:0110060
  • amelogenesis imperfecta hypomaturation type 2A2
  • Aliases:
    • AI2A2
    • amelogenesis imperfecta hypomaturation type IIA2
    • amelogenesis imperfecta pigmented hypomaturation type 2
    • amelogenesis imperfecta type IIA2
Homo sapiens (human)
DOID:0110053
  • amelogenesis imperfecta type 4
  • Aliases:
    • AI4
    • AIHHT
    • amelogenesis imperfecta hypomaturation-hypoplastic type with taurodontism
Homo sapiens (human)
DOID:0110054
  • amelogenesis imperfecta type 1A
  • Aliases:
    • AI1A
    • amelogenesis imperfecta hypoplastic type IA
    • amelogenesis imperfecta type IA
Homo sapiens (human)
DOID:0110061
  • amelogenesis imperfecta hypomaturation type 2A3
  • Aliases:
    • AI2A3
    • amelogenesis imperfecta hypomaturation type IIA3
    • amelogenesis imperfecta type IIA3
Homo sapiens (human)
DOID:0110056
  • amelogenesis imperfecta type 1C
  • Aliases:
    • AI1C
    • amelogenesis imperfecta type IC
    • autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion
    • autosomal recessive amelogenesis imperfecta local hypoplastic type
Homo sapiens (human)
DOID:4154
  • dentinogenesis imperfecta
Homo sapiens (human)
DOID:0110062
  • amelogenesis imperfecta hypomaturation type 2A4
  • Aliases:
    • AI2A4
    • amelogenesis imperfecta hypomaturation type IIA4
    • amelogenesis imperfecta type IIA4
Homo sapiens (human)
DOID:0110064
  • amelogenesis imperfecta type 1H
  • Aliases:
    • AI1H
    • amelogenesis imperfecta type IH
Homo sapiens (human)
DOID:0110065
  • amelogenesis imperfecta type 1F
  • Aliases:
    • AI1F
    • amelogenesis imperfecta hypoplastic type IF
    • amelogenesis imperfecta type IF
Homo sapiens (human)
DOID:0110052
  • amelogenesis imperfecta type 1B
  • Aliases:
    • AI1B
    • AIH2
    • amelogenesis imperfecta type IB
    • autosomal dominant hypoplastic local amelogenesis imperfecta
    • hereditary localized enamel hypoplasia
Homo sapiens (human)
DOID:10112
  • sleeping sickness
  • Aliases:
    • African sleeping sickness
    • African trypanosomiasis
Homo sapiens (human)
DOID:600
  • animal phobia
  • Aliases:
    • Fear of animals
    • Zoophobia
Homo sapiens (human)
DOID:599
  • specific phobia
  • Aliases:
    • simple phobia
Homo sapiens (human)

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Last updated: August 19, 2024