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 6576 - 6600 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:5077
  • subependymal giant cell astrocytoma
  • Aliases:
    • SEGA
Homo sapiens (human)
DOID:7007
  • childhood cerebral astrocytoma
  • Aliases:
    • pediatric astrocytoma of Cerebrum
Homo sapiens (human)
DOID:7008
  • protoplasmic astrocytoma
  • Aliases:
    • Protoplasmic Astrocytic tumor
Homo sapiens (human)
DOID:3078
  • anaplastic astrocytoma
  • Aliases:
    • grade III Astrocytic tumor
    • grade III astrocytoma
Homo sapiens (human)
DOID:7005
  • gemistocytic astrocytoma
  • Aliases:
    • Gemistocytic Astrocytic tumor
Homo sapiens (human)
DOID:6811
  • juvenile pilocytic astrocytoma
Homo sapiens (human)
DOID:4851
  • pilocytic astrocytoma
  • Aliases:
    • Piloid astrocytoma
    • grade I Astrocytic tumor
Homo sapiens (human)
DOID:6726
  • fibrillary astrocytoma
  • Aliases:
    • Fibrillary Astrocytic tumors
Homo sapiens (human)
DOID:3069
  • malignant astrocytoma
  • Aliases:
    • Astrocytic tumor
    • astrocytoma of Cerebrum
    • astrocytoma of brain
    • astroglioma
    • cerebral astrocytoma
Homo sapiens (human)
DOID:4543
  • retrograde amnesia
Homo sapiens (human)
DOID:480
  • movement disease
Homo sapiens (human)
DOID:11577
  • Cauda equina syndrome
Homo sapiens (human)
DOID:12143
  • neurogenic bladder
  • Aliases:
    • Neuropathic bladder
    • neurogenic dysfunction of the urinary bladder
    • neurogenic urinary bladder disorder
Homo sapiens (human)
DOID:2786
  • cerebellar disease
Homo sapiens (human)
DOID:0050753
  • cerebellar ataxia
Homo sapiens (human)
DOID:543
  • dystonia
  • Aliases:
    • dystonic disease
Homo sapiens (human)
DOID:9820
  • central gyrate choroidal dystrophy
  • Aliases:
    • Choroidal dystrophy, serpiginous
Homo sapiens (human)
DOID:2983
  • anuria
  • Aliases:
    • Suppression of urinary secretion
Homo sapiens (human)
DOID:0111131
  • focal segmental glomerulosclerosis 6
  • Aliases:
    • FSGS6
Homo sapiens (human)
DOID:0060610
  • megacystis-microcolon-intestinal hypoperistalsis syndrome
  • Aliases:
    • Berdon syndrome
    • Megacystis microcolon intestinal hypoperistalsis syndrome
    • megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH
    • visceral myopathy
Homo sapiens (human)
DOID:0111128
  • focal segmental glomerulosclerosis 1
  • Aliases:
    • FSGS1
Homo sapiens (human)
DOID:0111129
  • focal segmental glomerulosclerosis 2
  • Aliases:
    • FSGS2
Homo sapiens (human)
DOID:0111130
  • focal segmental glomerulosclerosis 5
  • Aliases:
    • FSGS5
Homo sapiens (human)
DOID:0060550
  • ablepharon macrostomia syndrome
Homo sapiens (human)
DOID:0111425
  • restrictive cardiomyopathy 1
  • Aliases:
    • RCM1
    • familial restrictive cardiomyopathy 1
Homo sapiens (human)

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Last updated: August 19, 2024