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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 6351 - 6375 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:10581
  • metachromatic leukodystrophy
  • Aliases:
    • MLD
    • Scholz cerebral sclerosis
    • arylsulfatase A deficiency
    • deficiency of cerebroside-sulfatase
    • sulfatide lipoidosis
Homo sapiens (human)
DOID:0060453
  • Reis-Bucklers corneal dystrophy
  • Aliases:
    • RBCD
    • anterior limiting membrane dystrophy type I
    • corneal dystrophy of Bowman layer type I
    • geographic corneal dystrophy
    • granular corneal dystrophy type III
Saccharomyces cerevisiae S288C
DOID:13001
  • carotid stenosis
  • Aliases:
    • Carotid artery stenosis
    • Stenosis, carotid artery
Homo sapiens (human)
DOID:0112209
  • developmental and epileptic encephalopathy 73
  • Aliases:
    • DEE73
    • early infantile epileptic encephalopathy 73
Rattus norvegicus (Norway rat)
DOID:0111274
  • CODAS syndrome
  • Aliases:
    • cerebral, ocular, dental, auricular, and skeletal syndrome
    • cerebro-oculo-dento-auriculo-skeletal syndrome
Homo sapiens (human)
DOID:0080263
  • autosomal recessive nonsyndromic deafness 108
Caenorhabditis elegans
DOID:422
  • congenital structural myopathy
Mus musculus (house mouse)
DOID:10605
  • short bowel syndrome
  • Aliases:
    • acquired short bowel syndrome
    • short gut syndrome
Xenopus tropicalis (tropical clawed frog)
DOID:0110943
  • autosomal recessive osteopetrosis 2
  • Aliases:
    • OPTB2
    • mild autosomal recessive form osteopetrosis
    • osteoclast-poor osteopetrosis
Homo sapiens (human)
DOID:0110175
  • Charcot-Marie-Tooth disease axonal type 2O
  • Aliases:
    • Charcot-Marie-Tooth neuropathy axonal type 2O
    • autosomal dominant Charcot-Marie-Tooth disease type 2O
    • autosomal dominant axonal Charcot-Marie-Tooth disease type 2O
Rattus norvegicus (Norway rat)
DOID:12720
  • cerebral atherosclerosis
Homo sapiens (human)
DOID:8029
  • sporadic breast cancer
Rattus norvegicus (Norway rat)
DOID:0050471
  • Carney complex
  • Aliases:
    • Carney Complex, Type 1
    • Carney Complex, Type 2
    • Carney Syndrome
    • Carney complex variant
    • LAMB Syndrome
    • NAME Syndrome
Homo sapiens (human)
DOID:1555
  • urticaria
Homo sapiens (human)
DOID:11168
  • anogenital venereal wart
  • Aliases:
    • Anogenital Human papilloma Virus Infectious Disease
    • Anogenital warts
    • Genital warts
    • genital wart virus infectious disease
    • venereal wart
Mus musculus (house mouse)
DOID:0090078
  • hypogonadotropic hypogonadism 7 with or without anosmia
Homo sapiens (human)
DOID:0050585
  • congenital generalized lipodystrophy
Homo sapiens (human)
DOID:13580
  • cholestasis
  • Aliases:
    • Obstruction of bile duct
    • bile occlusion
Saccharomyces cerevisiae S288C
DOID:0060537
  • mitochondrial complex II deficiency
  • Aliases:
    • isolated mitochondrial respiratory chain complex II deficiency
    • isolated succinate-CoQ reductase deficiency
    • isolated succinate-coenzyme Q reductase deficiency
    • isolated succinate-ubiquinone reductase deficiency
Rattus norvegicus (Norway rat)
DOID:0070437
  • hyperphosphatasia with impaired intellectual development syndrome 6
  • Aliases:
    • GPIBD40
    • HPMRS4
    • glycosylphosphatidylinositol biosynthesis defect 40
    • hyperphosphatasia with mental retardation syndrome 4
Homo sapiens (human)
DOID:0110722
  • neuronal ceroid lipofuscinosis 7
  • Aliases:
    • CLN7
Xenopus laevis (African clawed frog)
DOID:0110386
  • retinitis pigmentosa 42
  • Aliases:
    • RP42
Homo sapiens (human)
DOID:9146
  • visceral leishmaniasis
  • Aliases:
    • Infection by visceral leishmaniasis
    • Kala-Azar
Rattus norvegicus (Norway rat)
DOID:8692
  • myeloid leukemia
  • Aliases:
    • Non-Lymphocytic Leukemia
    • leukaemia myelogenous
    • leukemia myelogenous
    • myeloid granulocytic leukaemia
    • myeloid granulocytic leukemia
    • myeloid leukaemia
Xenopus tropicalis (tropical clawed frog)
DOID:0081301
  • intellectual developmental disorder with ocular anomalies and distinctive facial features
  • Aliases:
    • IDDOF
    • MTSS2-related neurodevelopmental disorder
Homo sapiens (human)
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Last updated: December 9, 2024