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 6526 - 6550 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:1561
  • cognitive disorder
  • Aliases:
    • cognitive disease
Homo sapiens (human)
DOID:1002
  • endometritis
Homo sapiens (human)
DOID:13487
  • childhood disintegrative disease
  • Aliases:
    • Disintegrative psychosis
    • Heller's syndrome
    • Symbiotic psychosis
Homo sapiens (human)
DOID:0050458
  • juvenile myelomonocytic leukemia
Homo sapiens (human)
DOID:649
  • prion disease
  • Aliases:
    • Prion disease pathway
    • Prion protein disease
    • Spongiform Encephalopathy
    • prion induced disorder
    • transmissible spongiform encephalopathy
Homo sapiens (human)
DOID:422
  • congenital structural myopathy
Homo sapiens (human)
DOID:14717
  • centronuclear myopathy
  • Aliases:
    • myotubular myopathy
Homo sapiens (human)
DOID:0070128
  • congenital nongoitrous hypothyroidism 6
  • Aliases:
    • CHNG6
Homo sapiens (human)
DOID:0070125
  • congenital nongoitrous hypothyroidism 5
  • Aliases:
    • CHNG5
Homo sapiens (human)
DOID:0070124
  • congenital nongoitrous hypothyroidism 2
  • Aliases:
    • CHNG2
    • congenital hypothyroidism due to thyroid dysgenesis or hypoplasia
Homo sapiens (human)
DOID:0070126
  • congenital nongoitrous hypothyroidism 1
  • Aliases:
    • CHNG1
    • TSH resistance
Homo sapiens (human)
DOID:0070127
  • congenital nongoitrous hypothyroidism 3
  • Aliases:
    • CHNG3
Homo sapiens (human)
DOID:0111140
  • IGSF1 deficiency syndrome
  • Aliases:
    • CHTE
    • X-linked central congenital hypothyroidism with late-onset macroorchidism
    • X-linked central congenital hypothyroidism with late-onset testicular enlargement
    • central hypothyroidism and testicular enlargement
Homo sapiens (human)
DOID:4249
  • Gerstmann-Straussler-Scheinker syndrome
  • Aliases:
    • Gerstmann-Straussler-Scheinker disease
    • PRION DEMENTIA
Homo sapiens (human)
DOID:14175
  • von Hippel-Lindau disease
  • Aliases:
    • Hippel Lindau syndrome
    • von Hippel-Lindau syndrome
Homo sapiens (human)
DOID:3852
  • Peutz-Jeghers syndrome
  • Aliases:
    • Colonic hamartomatous polyp
    • Peutz Jeghers colon polyp
    • Peutz Jeghers polyp
    • Peutz-Jeghers polyp of small Intestine
    • gastric Peutz-Jeghers polyp
    • peutz-jeghers small bowel hamartoma
Homo sapiens (human)
DOID:437
  • myasthenia gravis
Homo sapiens (human)
DOID:0060194
  • amyotrophic lateral sclerosis type 2
  • Aliases:
    • ALS2
    • amyotrophic lateral sclerosis 2
    • amyotrophic lateral sclerosis 2, juvenile
Homo sapiens (human)
DOID:0060196
  • amyotrophic lateral sclerosis type 4
  • Aliases:
    • ALS 4
    • amyotrophic lateral sclerosis 4
    • amyotrophic lateral sclerosis 4, juvenile
    • dHMN with upper motor neuron signs
    • distal hereditary motor neuropathy with pyramidal features
    • distal hereditary motor neuropathy with upper motor neuron signs
Homo sapiens (human)
DOID:231
  • motor neuron disease
Homo sapiens (human)
DOID:230
  • lateral sclerosis
  • Aliases:
    • adult-onset primary lateral sclerosis
    • primary lateral sclerosis
Homo sapiens (human)
DOID:0111064
  • autosomal recessive distal hereditary motor neuronopathy 1
  • Aliases:
    • DSMA1
    • SIANRF
    • SMARD1
    • autosomal recessive distal spinal muscular atrophy 1
    • autosomal recessive spinal muscular atrophy with respiratory distress
    • dHMN6
    • diaphragmatic spinal muscular atrophy
    • distal hereditary motor neuropathy type 6
    • distal spinal muscular atrophy 1
    • distal-HMN type 6
    • severe infantile axonal neuropathy with respiratory failure type 1
    • spinal muscular atrophy with respiratory distress type 1
Homo sapiens (human)
DOID:4873
  • anterior horn cell disease
Homo sapiens (human)
DOID:12377
  • spinal muscular atrophy
Homo sapiens (human)
DOID:11100
  • Q fever
  • Aliases:
    • Infection due to Coxiella burnetii
Homo sapiens (human)

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Last updated: August 19, 2024