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 5226 - 5250 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism
DOID:13399
  • color blindness
  • Aliases:
    • BLINDNESS COLOR
    • Colour blindness
    • Colour vision deficiency
Homo sapiens (human)
DOID:13911
  • achromatopsia
  • Aliases:
    • ACHM
    • Monochromatism
Homo sapiens (human)
DOID:0060179
  • Renpenning syndrome
  • Aliases:
    • Golabi-Ito-Hall syndrome
    • Sutherland-Haan X-linked mental retardation syndrome
    • X-linked intellectual disability due to PQBP1 mutations
    • X-linked intellectual disability, Renpenning type
    • X-linked mental retardation Renpenning type
    • X-linked mental retardation with spastic diplegia
    • syndromic X-linked mental retardation 8
Homo sapiens (human)
DOID:582
  • hemoglobinuria
Homo sapiens (human)
DOID:8747
  • obsolete subacute myeloid leukemia
Homo sapiens (human)
DOID:0080483
  • peroxisome biogenesis disorder 8A
  • Aliases:
    • peroxisome biogenesis disorder 8A (Zellweger)
Homo sapiens (human)
DOID:0060346
  • Native American myopathy
  • Aliases:
    • Bailey-Bloch congenital myopathy
    • congenital myopathy 13
Homo sapiens (human)
DOID:3262
  • phagocyte bactericidal dysfunction
  • Aliases:
    • phagocytic dysfunction
Homo sapiens (human)
DOID:12919
  • Plasmodium ovale malaria
  • Aliases:
    • Malariaby Plasmodium ovale
    • Ovale malaria
Homo sapiens (human)
DOID:11726
  • Emery-Dreifuss muscular dystrophy
  • Aliases:
    • EDMD
Homo sapiens (human)
DOID:0081331
  • glycogen storage disease Ic
Homo sapiens (human)
DOID:0081330
  • glycogen storage disease Ib
Homo sapiens (human)
DOID:1936
  • atherosclerosis
Rattus norvegicus (Norway rat)
DOID:418
  • systemic scleroderma
  • Aliases:
    • Scleroderma
    • Scleroderma syndrome
    • progressive systemic sclerosis
    • systemic sclerosis
Rattus norvegicus (Norway rat)
DOID:13603
  • obstructive jaundice
  • Aliases:
    • Cholestatic Jaundice
    • Cholestatic jaundice syndrome
    • Obstructive hyperbilirubinemia
Rattus norvegicus (Norway rat)
DOID:10908
  • hydrocephalus
  • Aliases:
    • hydrocephalus, X-linked
    • hydrocephalus, nonsyndromic, autosomal recessive
Rattus norvegicus (Norway rat)
DOID:1338
  • congenital dyserythropoietic anemia
  • Aliases:
    • congenital dyshaematopoietic anaemia
Rattus norvegicus (Norway rat)
DOID:0111218
  • Friedreich ataxia 1
  • Aliases:
    • FA1
    • FRDA1
Homo sapiens (human)
DOID:0111949
  • immunodeficiency 36
  • Aliases:
    • IMD36
    • activated phosphoinositide 3-kinase delta syndrome 2
Rattus norvegicus (Norway rat)
DOID:7305
  • astroblastoma
Rattus norvegicus (Norway rat)
DOID:5409
  • lung small cell carcinoma
Rattus norvegicus (Norway rat)
DOID:14179
  • X-linked agammaglobulinemia
  • Aliases:
    • BTK deficiency
    • Bruton agammaglobulinemia tyrosine kinase deficiency
    • Bruton disease
    • Bruton's Sex-Linked Agammaglobulinemia
    • Bruton's agammaglobulinaemia
    • Bruton's type agammaglobulinemia
    • Bruton-type agammaglobulinemia
Rattus norvegicus (Norway rat)
DOID:0081139
  • agammaglobulinemia 7
Rattus norvegicus (Norway rat)
DOID:0111454
  • SHORT syndrome
  • Aliases:
    • Aarskog-Ose-Pande syndrome
    • Lipodystrophy-Rieger anomaly-diabetes syndrome
    • Rieger anomaly-partial lipodystrophy syndrome
    • short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly, and teething delay
Rattus norvegicus (Norway rat)
DOID:12554
  • hemolytic-uremic syndrome
  • Aliases:
    • haemolytic-uraemic syndrome
    • hemolytic uremic syndrome
Rattus norvegicus (Norway rat)

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Last updated: August 19, 2024