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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 6876 - 6900 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0111274
  • CODAS syndrome
  • Aliases:
    • cerebral, ocular, dental, auricular, and skeletal syndrome
    • cerebro-oculo-dento-auriculo-skeletal syndrome
Mus musculus (house mouse)
DOID:0110355
  • retinitis pigmentosa 32
  • Aliases:
    • RP32
Homo sapiens (human)
DOID:4194
  • glucose metabolism disease
  • Aliases:
    • disorder of glucose metabolism
Saccharomyces cerevisiae S288C
DOID:9352
  • type 2 diabetes mellitus
  • Aliases:
    • NIDDM
    • insulin resistance
    • non-insulin-dependent diabetes mellitus
    • type 2 diabetes
    • type II diabetes mellitus
Caenorhabditis elegans
DOID:0060222
  • Scheie syndrome
  • Aliases:
    • mucopolysaccharidosis type 1S
    • mucopolysaccharidosis type IS
    • mucopolysaccharidosis type V
Homo sapiens (human)
DOID:6683
  • X-linked Aarskog syndrome
  • Aliases:
    • Aarskog-Scott syndrome
    • Greig's syndrome
Homo sapiens (human)
DOID:12932
  • endomyocardial fibrosis
  • Aliases:
    • African endomyocardial fibrosis
    • Becker's disease
    • Endomyocardial sclerosis
    • obscure African cardiomyopathy
Xenopus tropicalis (tropical clawed frog)
DOID:7474
  • malignant pleural mesothelioma
  • Aliases:
    • malignant mesothelioma of pleura
Saccharomyces cerevisiae S288C
DOID:0111630
  • familial erythrocytosis 8
  • Aliases:
    • BPGM deficiency
    • DPGM deficiency
    • ECYT8
    • bisphosphoglycerate mutase deficiency
    • bisphosphoglyceromutase deficiency
    • diphosphoglycerate mutase deficiency of erythrocyte
    • hemolytic anemia due to diphosphoglycerate mutase deficiency
Saccharomyces cerevisiae S288C
DOID:321
  • tropical spastic paraparesis
  • Aliases:
    • HTLV-associated myelopathy
    • Tropical spastic paralysis
    • Tropical spastic paraplegia
Mus musculus (house mouse)
DOID:1933
  • Rubinstein-Taybi syndrome
  • Aliases:
    • Broad Thumb-Hallux syndrome
    • Rubinstein syndrome
    • proximal chromosome 16p13.3 deletion syndrome
Homo sapiens (human)
DOID:2876
  • laryngeal squamous cell carcinoma
  • Aliases:
    • Epidermoid carcinoma of the Larynx
    • squamous cell carcinoma of larynx
Homo sapiens (human)
DOID:3125
  • multiple endocrine neoplasia
  • Aliases:
    • Multiple endocrine adenomatosis
    • Multiple endocrine neoplasia syndrome
Rattus norvegicus (Norway rat)
DOID:0070450
  • mitochondrial DNA depletion syndrome 19
Mus musculus (house mouse)
DOID:0090014
  • severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive
  • Aliases:
    • autosomal recessive T cell-negative, B-cell positive, NK cell-positive SCID
Mus musculus (house mouse)
DOID:13810
  • familial hypercholesterolemia
  • Aliases:
    • Fredrickson type IIa hyperlipoproteinemia
    • Fredrickson type IIa lipidaemia
    • familial hyperbetalipoproteinaemia
    • familial hypercholesteremia
    • hyperbetalipoproteinemia
    • type II hyperlipidemia
Danio rerio (zebrafish)
DOID:0110150
  • Charcot-Marie-Tooth disease type 1D
  • Aliases:
    • CMT1D
    • Charcot-Marie-Tooth neuropathy type 1D
    • HMSN ID
    • HMSN1D
    • hereditary motor and sensory neuropathy 1D
Homo sapiens (human)
DOID:0090084
  • hypogonadotropic hypogonadism 5 with or without anosmia
Drosophila melanogaster (fruit fly)
DOID:841
  • extrinsic allergic alveolitis
  • Aliases:
    • alveolitis
    • hypersensitivity pneumonitis
Drosophila melanogaster (fruit fly)
DOID:0060213
  • frontotemporal dementia and/or amyotrophic lateral sclerosis 1
  • Aliases:
    • ALSFTD
    • FTDALS1
    • FTDMND
    • amyotrophic lateral sclerosis and/or frontotemporal dementia
    • frontotemporal dementia and/or motor neuron disease
Homo sapiens (human)
DOID:0060856
  • right atrial isomerism
  • Aliases:
    • Ivemark syndrome
    • asplenia with cardiovascular anomalies
Homo sapiens (human)
DOID:9498
  • pulmonary eosinophilia
Rattus norvegicus (Norway rat)
DOID:0050117
  • disease by infectious agent
  • Aliases:
    • infectious disease
Homo sapiens (human)
DOID:4001
  • ovarian carcinoma
Danio rerio (zebrafish)
DOID:2115
  • B cell deficiency
  • Aliases:
    • B cell (antibody) deficiencies
    • Immunoglobulin heavy chain deficiency
    • immunoglobulin heavy chain deletion
Mus musculus (house mouse)
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Last updated: December 9, 2024