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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 15651 - 15675 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0080591
  • Klippel-Feil syndrome 3
Xenopus laevis (African clawed frog)
DOID:5485
  • synovial sarcoma
Homo sapiens (human)
DOID:0080411
  • familial adenomatous polyposis 3
Caenorhabditis elegans
DOID:11994
  • atrophy of testis
Homo sapiens (human)
DOID:1826
  • epilepsy
  • Aliases:
    • epilepsy syndrome
    • epileptic syndrome
Rattus norvegicus (Norway rat)
DOID:0110358
  • retinitis pigmentosa 12
  • Aliases:
    • RP12
Homo sapiens (human)
DOID:0111348
  • multiple epiphyseal dysplasia with myopia and deafness
  • Aliases:
    • EDMMD
    • multiple epiphyseal dysplasia, Beighton type
    • multiple epiphyseal dysplasia-myopia-deafness syndrome
Xenopus tropicalis (tropical clawed frog)
DOID:10123
  • pigmentation disease
Mus musculus (house mouse)
DOID:0060720
  • autosomal recessive congenital ichthyosis 11
  • Aliases:
    • IFAH syndrome
    • IHS
    • autosomal recessive ichthyosis with hypotrichosis
    • hypotrichosis-congenital ichthyosis syndrome
    • ichthyosis and follicular atrophoderma with hypotrichosis and hypohidrosis
    • ichthyosis-follicular atrophoderma-hypotrichosis syndrome
    • ichthyosis-follicular atrophoderma-hypotrichosis-hypohidrosis syndrome
    • ichthyosis-hypotrichosis syndrome
Homo sapiens (human)
DOID:62
  • aortic valve disease
Drosophila melanogaster (fruit fly)
DOID:0060713
  • autosomal recessive congenital ichthyosis 4B
  • Aliases:
    • ARCI4B
    • harlequin ichthyosis
    • harlequin type ichthyosis congenita
    • harlequin type ichthyosis fetalis
Saccharomyces cerevisiae S288C
DOID:0050809
  • mucopolysaccharidosis IX
Homo sapiens (human)
DOID:0080690
  • RASopathy
  • Aliases:
    • RAS/mitogen-activated protein kinase syndrome
Mus musculus (house mouse)
DOID:3304
  • germinoma
Rattus norvegicus (Norway rat)
DOID:0060781
  • congenital secretory sodium diarrhea 3
  • Aliases:
    • congenital secretory sodium diarrhea 3 syndromic
    • congenital secretory sodium diarrhea 3 with or without other congenital anomalies
    • congenital secretory sodium diarrhoea 3
    • congenital secretory sodium diarrhoea 3 syndromic
    • congenital secretory sodium diarrhoea 3 with or without other congenital anomalies
Homo sapiens (human)
DOID:10976
  • membranous glomerulonephritis
  • Aliases:
    • membranous nephropathy
Rattus norvegicus (Norway rat)
DOID:0060399
  • chromosome 16p12.1 deletion syndrome
Homo sapiens (human)
DOID:0050827
  • rheumatic heart disease
  • Aliases:
    • rheumatic carditis
Mus musculus (house mouse)
DOID:0070028
  • APP-related cerebral amyloid angiopathy
  • Aliases:
    • Amyloidosis, Cerebroarterial, App-Related
    • Amyloidosis, Hereditary, With Cerebral Hemorrhage, Dutch Variant
    • Cerebral Amyloid Angiopathy, App-Related, Arctic Variant
    • Cerebral Amyloid Angiopathy, App-Related, Dutch Variant
    • Cerebral Amyloid Angiopathy, App-Related, Flemish Variant
    • Cerebral Amyloid Angiopathy, App-Related, Iowa Variant
    • Cerebral Amyloid Angiopathy, App-Related, Italian Variant
    • HCHWAD
Caenorhabditis elegans
DOID:0080010
  • bone structure disease
Homo sapiens (human)
DOID:150
  • disease of mental health
Mus musculus (house mouse)
DOID:0080762
  • autosomal recessive limb-girdle muscular dystrophy type 2Z
  • Aliases:
    • limb-girdle muscular dystrophy 21
Homo sapiens (human)
DOID:2219
  • Glanzmann's thrombasthenia
  • Aliases:
    • BDPLT2
    • Glanzmann thrombasthenia
    • Glycoprotein IIb/IIIa defect
    • Thrombocytasthenia
    • deficiency of GP IIb-IIIa complex
    • deficiency of glycoprotein complex IIb-IIIa
    • deficiency of platelet fibrinogen receptor
    • platelet glycoprotein IIb-IIIa deficiency
    • platelet-type bleeding disorder 2
    • thrombasthenia of Glanzmann and Naegeli
Drosophila melanogaster (fruit fly)
DOID:13099
  • Moyamoya disease
  • Aliases:
    • progressive intracranial arterial occlusion
Homo sapiens (human)
DOID:3905
  • lung carcinoma
  • Aliases:
    • cancer of lung
Saccharomyces cerevisiae S288C
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Last updated: December 9, 2024