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 1151 - 1175 of 4621 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:0110041
  • Alzheimer's disease 8
  • Aliases:
    • AD8
    • Alzheimer disease 8
    • Alzheimer disease, familial 8
    • Alzheimer's disease 8, late onset
Homo sapiens (human)
DOID:0110042
  • Alzheimer's disease 3
  • Aliases:
    • AD3
    • Alzheimer disease 3
    • Alzheimer disease 3, early onset
    • Alzheimer disease familial 3
Homo sapiens (human)
DOID:0110043
  • Alzheimer's disease 10
  • Aliases:
    • AD10
    • Alzheimer disease 10
    • Alzheimer disease familial 10
    • Alzheimer's disease 10, early onset
Homo sapiens (human)
DOID:0110044
  • Alzheimer's disease 11
  • Aliases:
    • AD11
    • Alzheimer disease 11
    • Alzheimer's disease 11, late onset
Homo sapiens (human)
DOID:0110045
  • Alzheimer's disease 12
  • Aliases:
    • AD12
    • Alzheimer disease 12
    • Alzheimer disease familial 12
Homo sapiens (human)
DOID:0110046
  • Alzheimer's disease 13
  • Aliases:
    • AD13
    • Alzheimer disease 13
    • Alzheimer's disease 13, late onset
Homo sapiens (human)
DOID:0110047
  • Alzheimer's disease 14
  • Aliases:
    • AD14
    • Alzheimer disease 14
    • Alzheimer's disease 14, late onset
Homo sapiens (human)
DOID:0110048
  • Alzheimer's disease 15
  • Aliases:
    • AD15
    • Alzheimer disease 15
    • Alzheimer's disease 15, late onset
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: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: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: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:0110057
  • amelogenesis imperfecta type 2A1
  • Aliases:
    • AI2A1
    • amelogenesis imperfecta pigmented hypomaturation type 1
    • amelogenesis imperfecta type IIA1
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: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: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:0110061
  • amelogenesis imperfecta hypomaturation type 2A3
  • Aliases:
    • AI2A3
    • amelogenesis imperfecta hypomaturation type IIA3
    • amelogenesis imperfecta type IIA3
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:0110063
  • amelogenesis imperfecta hypomaturation type 2A5
  • Aliases:
    • AI2A5
    • amelogenesis imperfecta hypomaturation type IIA5
    • amelogenesis imperfecta type IIA5
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: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:0110078
  • Leber congenital amaurosis 1
  • Aliases:
    • LCA1
    • amaurosis congenita of Leber I
Homo sapiens (human)
DOID:0110096
  • short-rib thoracic dysplasia 14 with polydactyly
  • Aliases:
    • SRTD14
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024