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 2651 - 2675 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0070342
  • adult-onset type II citrullinemia
  • Aliases:
    • citrin deficiency
Drosophila melanogaster (fruit fly)
DOID:4137
  • common bile duct disease
Drosophila melanogaster (fruit fly)
DOID:0070302
  • multiple epiphyseal dysplasia 7
  • Aliases:
    • EDM7
Caenorhabditis elegans
DOID:0060462
  • Desbuquois dysplasia
  • Aliases:
    • Desbuquois syndrome
    • micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification
Caenorhabditis elegans
DOID:0050568
  • spondylocostal dysostosis
  • Aliases:
    • Jarcho-Levin syndrome
    • costovertebral dysplasia
    • spondylothoracic dysostosis
    • spondylothoracic dysplasia
Caenorhabditis elegans
DOID:0112365
  • spondylocostal dysostosis 1
  • Aliases:
    • SCDO1
    • autosomal recessive spondylocostal dysostosis 1
Caenorhabditis elegans
DOID:162
  • cancer
  • Aliases:
    • malignant neoplasm
    • malignant tumor
    • primary cancer
Caenorhabditis elegans
DOID:1934
  • dysostosis
Caenorhabditis elegans
DOID:0060350
  • adenine phosphoribosyltransferase deficiency
  • Aliases:
    • 2,8-dihydroxyadenine urolithiasis
    • APRT deficiency
Caenorhabditis elegans
DOID:1919
  • Lesch-Nyhan syndrome
  • Aliases:
    • Complete hypoxanthine-guanine phosphoribosyltransferase deficiency
    • HG-PRT deficiency
    • Hypoxanthine-guanine phosphoribosyltransferase deficiency
    • Hypoxanthine-guanine-phosphoribosyltransferase deficiency
    • Lesch - Nyhan syndrome
    • X-linked hyperuricemia
    • deficiency of IMP pyrophosphorylase
    • hypoxanthine guanine phosphoribosyltransferase deficiency
Caenorhabditis elegans
DOID:0050850
  • diabetic encephalopathy
Caenorhabditis elegans
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:0080348
  • Alzheimer's disease 1
  • Aliases:
    • Alzheimer's disease 1, early onset
Caenorhabditis elegans
DOID:1289
  • neurodegenerative disease
  • Aliases:
    • degenerative disease
Caenorhabditis elegans
DOID:2280
  • hidradenitis suppurativa
  • Aliases:
    • Acne inversa, familial
Caenorhabditis elegans
DOID:0110698
  • hypotrichosis 1
  • Aliases:
    • Hhs
    • Hts
    • Hypt1
    • hereditary generalized hypotrichosis simplex
Xenopus laevis (African clawed frog)
DOID:0110698
  • hypotrichosis 1
  • Aliases:
    • Hhs
    • Hts
    • Hypt1
    • hereditary generalized hypotrichosis simplex
Xenopus tropicalis (tropical clawed frog)
DOID:1338
  • congenital dyserythropoietic anemia
  • Aliases:
    • congenital dyshaematopoietic anaemia
Caenorhabditis elegans
DOID:3413
  • alpha-mannosidosis
  • Aliases:
    • Alpha-D-mannosidosis
    • alpha-mannosidase deficiency
    • deficiency of alpha-mannosidase
Caenorhabditis elegans
DOID:0081097
  • Rafiq syndrome
  • Aliases:
    • MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
Drosophila melanogaster (fruit fly)
DOID:1338
  • congenital dyserythropoietic anemia
  • Aliases:
    • congenital dyshaematopoietic anaemia
Drosophila melanogaster (fruit fly)
DOID:0080564
  • congenital disorder of glycosylation Il
  • Aliases:
    • congenital disorder of glycosylation 1l
Caenorhabditis elegans
DOID:0080560
  • congenital disorder of glycosylation Ih
  • Aliases:
    • congenital disorder of glycosylation 1h
Caenorhabditis elegans
DOID:0110676
  • congenital myasthenic syndrome 13
  • Aliases:
    • CMS13
    • CMSTA2
    • congenital myasthenic syndrome 13 with tubular aggregates
    • congenital myasthenic syndrome with tubular aggregates 2
Caenorhabditis elegans
DOID:0080562
  • congenital disorder of glycosylation Ij
  • Aliases:
    • Congenital disorder of glycosylation 1j
Caenorhabditis elegans

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Last updated: December 9, 2024