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 October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 3326 - 3350 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:3326
  • purpura
  • Aliases:
    • Purpuric disorder
Rattus norvegicus (Norway rat)
DOID:10871
  • age related macular degeneration
  • Aliases:
    • Age Related Maculopathies
    • Age Related Maculopathy
    • Senile macular degeneration
    • Senile macular retinal degeneration
    • age-related macular degeneration
Rattus norvegicus (Norway rat)
DOID:11721
  • glycogen storage disease VII
  • Aliases:
    • Glycogen storage disease 7
    • Glycogen storage disease, type VII
    • Muscle phosphofructokinase deficiency
    • glycogen storage disease type VII
    • phosphofructokinase myopathy
Rattus norvegicus (Norway rat)
DOID:0070043
  • autosomal dominant intellectual developmental disorder 13
  • Aliases:
    • MRD13
    • autosomal dominant mental retardation 13
    • autosomal dominant non-syndromic intellectual disability 13
    • mental retardation, autosomal dominant 13, with neuronal migration defects
Rattus norvegicus (Norway rat)
DOID:9719
  • neovascular inflammatory vitreoretinopathy
  • Aliases:
    • ADNIV
    • Retinitis proliferans
    • autosomal dominant neovascular inflammatory vitreoretinopathy
    • proliferative vitreoretinopathy
Rattus norvegicus (Norway rat)
DOID:0050951
  • hereditary ataxia
Rattus norvegicus (Norway rat)
DOID:0070466
  • carpal tunnel syndrome 1
  • Aliases:
    • CTS1
Rattus norvegicus (Norway rat)
DOID:0050588
  • muscular dystrophy-dystroglycanopathy type B1
  • Aliases:
    • CMD due to dystroglycanopathy
    • Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B1
Rattus norvegicus (Norway rat)
DOID:2997
  • Sertoli-Leydig cell tumor
Rattus norvegicus (Norway rat)
DOID:0110739
  • neurodegeneration with brain iron accumulation 5
  • Aliases:
    • BPAN
    • Beta-Propeller Protein-Associated Neurodegeneration
    • NBIA5
    • SENDA
    • Static Encephalopathy Of Childhood With Neurodegeneration In Adulthood
Rattus norvegicus (Norway rat)
DOID:0080334
  • aortic valve disease 2
Rattus norvegicus (Norway rat)
DOID:11801
  • protein-energy malnutrition
Rattus norvegicus (Norway rat)
DOID:9975
  • cocaine dependence
Rattus norvegicus (Norway rat)
DOID:0050800
  • cerebral creatine deficiency syndrome 1
  • Aliases:
    • CEREBRAL CREATINE DEFICIENCY SYNDROME 1
    • SLC6A8 deficiency
    • creatine transporter deficiency
Rattus norvegicus (Norway rat)
DOID:0080286
  • spinocerebellar ataxia 44
Rattus norvegicus (Norway rat)
DOID:0110877
  • holoprosencephaly 11
  • Aliases:
    • HPE11
Rattus norvegicus (Norway rat)
DOID:0111843
  • Paganini-Miozzo syndrome
  • Aliases:
    • MRXSPM
Rattus norvegicus (Norway rat)
DOID:2277
  • gonadal disease
Rattus norvegicus (Norway rat)
DOID:0060884
  • renal hypomagnesemia 6
  • Aliases:
    • HOMG6
Rattus norvegicus (Norway rat)
DOID:0112069
  • nuclear type mitochondrial complex I deficiency 22
  • Aliases:
    • MC1DN22
Rattus norvegicus (Norway rat)
DOID:0080585
  • Van Maldergem syndrome 1
Rattus norvegicus (Norway rat)
DOID:0111373
  • familial progressive hyperpigmentation with or without hypopigmentation
  • Aliases:
    • FPHH
    • MUH
    • melanosis universalis hereditaria
Rattus norvegicus (Norway rat)
DOID:0110157
  • Charcot-Marie-Tooth disease type 2J
  • Aliases:
    • CMT2J
    • Charcot-Marie-Tooth disease type 2 with hearing loss and pupillary abnormalities
    • Charcot-Marie-Tooth neuropathy type 2J
Rattus norvegicus (Norway rat)
DOID:1289
  • neurodegenerative disease
  • Aliases:
    • degenerative disease
Rattus norvegicus (Norway rat)
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Rattus norvegicus (Norway rat)

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Last updated: December 9, 2024