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 5626 - 5650 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:0050524
  • maturity-onset diabetes of the young
  • Aliases:
    • MODY
    • Mason-type diabetes
Danio rerio (zebrafish)
DOID:0110741
  • type 1 diabetes mellitus 2
  • Aliases:
    • IDDM2
    • Insulin-Dependent Diabetes Mellitus 2
Danio rerio (zebrafish)
DOID:11717
  • neonatal diabetes
  • Aliases:
    • diabetes mellitus syndrome in newborn infant
    • neonatal diabetes mellitus
Danio rerio (zebrafish)
DOID:3587
  • pancreatic ductal carcinoma
  • Aliases:
    • malignant neoplasm of duct of Wirsung
    • pancreatic duct cancer
Danio rerio (zebrafish)
DOID:2018
  • hyperinsulinism
  • Aliases:
    • hyperinsulinemia
Danio rerio (zebrafish)
DOID:3892
  • insulinoma
  • Aliases:
    • Insulin-Producing tumor of Islet cells
    • Islet cell adenoma
Danio rerio (zebrafish)
DOID:11714
  • gestational diabetes
  • Aliases:
    • GDM
    • Gestational diabetes mellitus
    • Maternal gestational diabetes mellitus
Danio rerio (zebrafish)
DOID:0060639
  • permanent neonatal diabetes mellitus
  • Aliases:
    • PDMI
    • PNDM
    • permanent diabetes mellitus of infancy
Danio rerio (zebrafish)
DOID:1920
  • hyperuricemia
  • Aliases:
    • Blood urate raized
    • uricacidemia
Danio rerio (zebrafish)
DOID:0014667
  • disease of metabolism
  • Aliases:
    • metabolic disease
Danio rerio (zebrafish)
DOID:535
  • sleep disorder
  • Aliases:
    • Non-organic sleep disorder
Danio rerio (zebrafish)
DOID:4080
  • tricuspid valve insufficiency
  • Aliases:
    • Tricuspid incompetence
    • Tricuspid regurgitation
    • Tricuspid valve regurgitation
Homo sapiens (human)
DOID:0050476
  • Barth syndrome
  • Aliases:
    • 3-methylglutaconicaciduria type 2
    • 3-methylglutaconicaciduria type II
    • MGA Type 2
    • MGA type II
Homo sapiens (human)
DOID:13789
  • staphyloma posticum
Homo sapiens (human)
DOID:0080558
  • congenital disorder of glycosylation If
  • Aliases:
    • congenital disorder of glycosylation 1f
Rattus norvegicus (Norway rat)
DOID:0070215
  • familial hyperinsulinemic hypoglycemia 4
  • Aliases:
    • HHF4
    • hyperinsulinemic hypoglycemia due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
    • hyperinsulinism due to SCHAD deficiency
    • hyperinsulinism due to glutamodehydrogenase deficiency
    • hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency
Homo sapiens (human)
DOID:0112136
  • severe congenital neutropenia 4
  • Aliases:
    • Dursun syndrome
    • SCN4
    • autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
    • severe congenital neutropenia-pulmonary hypertension-superficial venous angiectasis syndrome
Rattus norvegicus (Norway rat)
DOID:0111235
  • congenital muscular dystrophy-dystroglycanopathy type A12
  • Aliases:
    • MDDGA12
    • Walker-Warburg syndrome or muscle-eye-brain disease POMK-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A12
Rattus norvegicus (Norway rat)
DOID:0112381
  • muscular dystrophy-dystroglycanopathy type C12
  • Aliases:
    • LGMD due to POMK deficiency
    • Limb-girdle muscular dystrophy due to POMK deficiency
    • MDDGC12
    • muscular dystrophy-dystroglycanopathy, limb-girdle, POMK-related
Rattus norvegicus (Norway rat)
DOID:0110242
  • cataract 13 with adult i phenotype
  • Aliases:
    • CTRCT13
Rattus norvegicus (Norway rat)
DOID:746
  • adenomatoid tumor
  • Aliases:
    • adenomatoid tumour
    • benign localised epithelial Mesothelioma
    • benign localized epithelial Mesothelioma
Homo sapiens (human)
DOID:13137
  • Werdnig-Hoffmann disease
  • Aliases:
    • HMN (Hereditary motor Neuropathy) Proximal type I
    • SMA1
    • Spinal muscular atrophy 1
    • hereditary motor neuropathy proximal type I
    • infantile muscular atrophy
    • progressive muscular atrophy of infancy
Homo sapiens (human)
DOID:0060160
  • childhood spinal muscular atrophy
  • Aliases:
    • spinal muscular atrophies of childhood
    • survival motor neuron spinal muscular atrophy
Homo sapiens (human)
DOID:12376
  • juvenile spinal muscular atrophy
  • Aliases:
    • Kugelberg-Welander disease
    • SMA3
    • Spinal Muscular Atrophy Type 3
    • Type III Spinal Muscular Atrophy
Homo sapiens (human)
DOID:1580
  • diffuse scleroderma
  • Aliases:
    • diffuse systemic sclerosis
    • systemic sclerosis, diffuse
Homo sapiens (human)

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Last updated: August 19, 2024