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 5901 - 5925 of 7942 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism
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:0110048
  • Alzheimer's disease 15
  • Aliases:
    • AD15
    • Alzheimer disease 15
    • Alzheimer's disease 15, 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:0110046
  • Alzheimer's disease 13
  • Aliases:
    • AD13
    • Alzheimer disease 13
    • Alzheimer's disease 13, late onset
Homo sapiens (human)
DOID:0110045
  • Alzheimer's disease 12
  • Aliases:
    • AD12
    • Alzheimer disease 12
    • Alzheimer disease familial 12
Homo sapiens (human)
DOID:0110044
  • Alzheimer's disease 11
  • Aliases:
    • AD11
    • Alzheimer disease 11
    • Alzheimer's disease 11, late onset
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:0110042
  • Alzheimer's disease 3
  • Aliases:
    • AD3
    • Alzheimer disease 3
    • Alzheimer disease 3, early onset
    • Alzheimer disease familial 3
Homo sapiens (human)
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:0110039
  • Alzheimer's disease 7
  • Aliases:
    • AD7
    • Alzheimer disease 7
    • Alzheimer disease, familial 7
Homo sapiens (human)
DOID:0110038
  • Alzheimer's disease 6
  • Aliases:
    • AD6
    • Alzheimer disease 6
    • Alzheimer disease 6, late onset
Homo sapiens (human)
DOID:0110037
  • Alzheimer's disease 5
  • Aliases:
    • AD5
    • Alzheimer disease 5
    • Alzheimer disease, familial 5
    • Alzheimer's disease 5, late onset
Homo sapiens (human)
DOID:0110035
  • Alzheimer's disease 2
  • Aliases:
    • AD2
    • Alzheimer disease 2, late onset
    • Alzheimer disease associated with APOE4
    • Alzheimer disease-2
Homo sapiens (human)
DOID:0110031
  • hemoglobin H disease
  • Aliases:
    • HBH
    • alpha thalassemia, haemoglobin H type
    • alpha thalassemia, hemoglobin H type
    • alpha-thalassemia intermedia
    • haemoglobin H disease
    • haemoglobin H disease, deletional
    • hemoglobin H disease, deletional
Homo sapiens (human)
DOID:0110030
  • alpha thalassemia-X-linked intellectual disability syndrome
  • Aliases:
    • ATR, nondeletion type
    • ATR-X syndrome
    • alpha-thalassemia/mental retardation syndrome nondeletion type
Homo sapiens (human)
DOID:0110029
  • alpha thalassemia-intellectual disability syndrome type 1
  • Aliases:
    • ATR syndrome linked to chromosome 16
    • ATR syndrome, deletion type
    • ATR-16 syndrome
    • alpha thalassemia-intellectual disability syndrome, deletion type
    • alpha thalassemia-retardation syndrome
    • alpha-thalassemia-intellectual disability syndrome linked to chromosome 16
    • alpha-thalassemia/mental retardation syndrome, deletion-type
    • alpha-thalassemia/mental retardation syndrome, type 1
Homo sapiens (human)
DOID:0110016
  • Leber congenital amaurosis 2
  • Aliases:
    • LCA2
    • amaurosis congenita of Leber II
Homo sapiens (human)
DOID:0110011
  • advanced sleep phase syndrome 1
  • Aliases:
    • FASPS1
    • familial advanced sleep phase syndrome 1
Mus musculus (house mouse)
DOID:0110011
  • advanced sleep phase syndrome 1
  • Aliases:
    • FASPS1
    • familial advanced sleep phase syndrome 1
Rattus norvegicus (Norway rat)
DOID:0110011
  • advanced sleep phase syndrome 1
  • Aliases:
    • FASPS1
    • familial advanced sleep phase syndrome 1
Homo sapiens (human)
DOID:0110008
  • achromatopsia 3
  • Aliases:
    • ACHM1
    • ACHM3
    • Pingelapese blindness
    • RMCH1
    • rod monochromacy 1
    • rod monochromatism 1
Homo sapiens (human)
DOID:0110006
  • 3-methylglutaconic aciduria type 4
  • Aliases:
    • 3-methylglutaconic aciduria type IV
    • MGA type IV
    • MGA4
    • MGCA4
Homo sapiens (human)
DOID:0110004
  • 3-methylglutaconic aciduria type 3
  • Aliases:
    • 3-methylglutaconic aciduria type III
    • Costeff optic atrophy syndrome
    • Costeff syndrome
    • Iraqi-Jewish optic atrophy plus
    • MGA3
    • autosomal recessive optic atrophy plus syndrome
    • autosomal recessive optic atrophy type 3
    • infantile optic atrophy with chorea and spastic paraplegia
Homo sapiens (human)
DOID:0090145
  • dopamine beta-hydroxylase deficiency
  • Aliases:
    • congenital dopamine beta-hydroxylase deficiency
    • noradrenaline deficiency
    • norepinephrine deficiency
Saccharomyces cerevisiae S288C
DOID:0090142
  • cystathioninuria
  • Aliases:
    • cystathionase deficiency
    • cystathione gamma-lyase deficiency syndrome
    • gamma-cystathionase deficiency
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024