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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 10201 - 10225 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:8398
  • osteoarthritis
  • Aliases:
    • Osteoarthrosis and allied disorder
    • degenerative arthritis
    • degenerative joint disease
    • hypertrophic arthritis
    • osteoarthrosis
Mus musculus (house mouse)
DOID:0110312
  • hypertrophic cardiomyopathy 6
  • Aliases:
    • CMH6
    • cardiomyopathy, familial hypertrophic 6
Mus musculus (house mouse)
DOID:0090125
  • brain small vessel disease 1
  • Aliases:
    • BSVD1
    • COL4A1-related brain small vessel disease with hemorrhage
    • COL4A1-related familial vascular leukoencephalopathy
    • COL4A1-related retinal arteriolar tortuosity-infantile hemiparesis-autosomal dominant leukoencephalopathy syndrome
    • autosomal dominant retinal arteriolar tortuosity, infantile hemiparesis, and leukencephalopathy
    • brain small vessel disease with Axenfeld-Riegar anomaly
    • brain small vessel disease with hemorrhage
    • brain small vessel disease with or without ocular anomalies
    • infantile hemiparesis
    • leukoencephalopathy with Axenfeld-Riegar anomaly
Mus musculus (house mouse)
DOID:9649
  • congenital nystagmus
Mus musculus (house mouse)
DOID:0080201
  • Peters plus syndrome
  • Aliases:
    • Krause-Kivlin syndrome
    • Peters anomaly-short limb dwarfism syndrome
    • Peters-plus syndrome
Mus musculus (house mouse)
DOID:0110214
  • cleft soft palate
  • Aliases:
    • cleft velum
    • cleft velum palatinum
    • soft cleft palate
Mus musculus (house mouse)
DOID:0080467
  • developmental and epileptic encephalopathy 2
  • Aliases:
    • DEE2
    • EIEE2
    • X-linked infantile spasm syndrome 2
    • early infantile epileptic encephalopathy 2
Mus musculus (house mouse)
DOID:0050591
  • tooth agenesis
  • Aliases:
    • familial tooth agenesis
    • hypodontia
    • oligodontia
    • selective tooth agenesis
Mus musculus (house mouse)
DOID:0050606
  • acrokeratosis verruciformis
  • Aliases:
    • Acrokeratosis verruciformis of Hopf
    • Hopf disease
Mus musculus (house mouse)
DOID:0081426
  • autosomal recessive distal hereditary motor neuronopathy 7
Mus musculus (house mouse)
DOID:9255
  • frontotemporal dementia
  • Aliases:
    • Wilhemsen-Lynch disease
    • frontotemporal lobar degeneration
    • multiple system tauopathy with presenile dementia
    • pallidopontonigral degeneration
Mus musculus (house mouse)
DOID:0060700
  • familial hypocalciuric hypercalcemia 1
  • Aliases:
    • FHH type 1
    • HHC1
    • familial benign hypercalcemia 1
    • familial hypocalciuric hypercalcemia type I
    • hypocalciuric hypercalcemia type I
Mus musculus (house mouse)
DOID:0111059
  • Bernard-Soulier syndrome type A2
  • Aliases:
    • BSSA2
Mus musculus (house mouse)
DOID:0080334
  • aortic valve disease 2
Mus musculus (house mouse)
DOID:14702
  • branchiootorenal syndrome
  • Aliases:
    • Branchio-Oto-renal syndrome
    • Branchio-otorenal dysplasia
    • Melnick-Fraser syndrome
    • branchiootorenal dysplasia
Mus musculus (house mouse)
DOID:2729
  • dyskeratosis congenita
  • Aliases:
    • DKCD
Mus musculus (house mouse)
DOID:225
  • syndrome
Mus musculus (house mouse)
DOID:8997
  • polycythemia vera
  • Aliases:
    • Osler-Vaquez syndrome
    • Polycythaemia rubra vera
    • Proliferative polycythaemia
    • chronic erythremia
Mus musculus (house mouse)
DOID:0050861
  • colorectal adenocarcinoma
Mus musculus (house mouse)
DOID:2615
  • papilloma
  • Aliases:
    • papillomatosis
Mus musculus (house mouse)
DOID:0110444
  • dilated cardiomyopathy 1X
  • Aliases:
    • CMD1X
    • dilated cardiomyopathy with mild or no proximal muscle weakness
Mus musculus (house mouse)
DOID:12986
  • leukostasis
Mus musculus (house mouse)
DOID:0112072
  • nuclear type mitochondrial complex I deficiency 20
  • Aliases:
    • ACAD9 deficiency
    • Acyl-CoA dehydrogenase 9 deficiency
    • MC1DN20
    • mitochondrial complex 1 deficiency due to ACAD9 deficiency
Mus musculus (house mouse)
DOID:0111517
  • autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2
  • Aliases:
    • PEOA2
    • autosomal dominant progressive external ophthalmoplegia 2
Mus musculus (house mouse)
DOID:0080006
  • bone development disease
Mus musculus (house mouse)
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Last updated: December 9, 2024