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 11226 - 11250 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:10983
  • Alport syndrome
  • Aliases:
    • Hereditary Nephritis
Drosophila melanogaster (fruit fly)
DOID:0060263
  • porencephaly
Drosophila melanogaster (fruit fly)
DOID:0110032
  • autosomal dominant Alport syndrome
Drosophila melanogaster (fruit fly)
DOID:0111365
  • benign familial hematuria
  • Aliases:
    • BFH
    • TMN
    • thin basement membrane nephropathy
    • thin membrane nephropathy
Drosophila melanogaster (fruit fly)
DOID:0111547
  • retinal arterial tortuosity
  • Aliases:
    • RATOR
    • retinal arteriolar tortuosity
    • retinal hemorrhage with vascular tortuosity
    • tortuosity of retinal arteries
Drosophila melanogaster (fruit fly)
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
Drosophila melanogaster (fruit fly)
DOID:0110034
  • X-linked Alport syndrome
  • Aliases:
    • nephropathy and deafness, X-linked
Drosophila melanogaster (fruit fly)
DOID:0110033
  • autosomal recessive Alport syndrome
Drosophila melanogaster (fruit fly)
DOID:13223
  • uterine fibroid
  • Aliases:
    • Plexiform leiomyoma
    • UTERUS FIBROMA
    • leiomyoma of Corpus Uteri
    • uterine leiomyoma
Drosophila melanogaster (fruit fly)
DOID:854
  • collagen disease
  • Aliases:
    • collagen disorder
Drosophila melanogaster (fruit fly)
DOID:423
  • myopathy
Drosophila melanogaster (fruit fly)
DOID:557
  • kidney disease
  • Aliases:
    • impaired renal function disease
    • nephropathy
Drosophila melanogaster (fruit fly)
DOID:0111547
  • retinal arterial tortuosity
  • Aliases:
    • RATOR
    • retinal arteriolar tortuosity
    • retinal hemorrhage with vascular tortuosity
    • tortuosity of retinal arteries
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:0060263
  • porencephaly
Mus musculus (house mouse)
DOID:13223
  • uterine fibroid
  • Aliases:
    • Plexiform leiomyoma
    • UTERUS FIBROMA
    • leiomyoma of Corpus Uteri
    • uterine leiomyoma
Mus musculus (house mouse)
DOID:854
  • collagen disease
  • Aliases:
    • collagen disorder
Mus musculus (house mouse)
DOID:14757
  • Ehlers-Danlos syndrome hypermobility type
  • Aliases:
    • Ehlers-Danlos syndrome, type 3
    • type III Ehlers-Danlos syndrome
Rattus norvegicus (Norway rat)
DOID:14756
  • vascular type Ehlers-Danlos syndrome
  • Aliases:
    • autosomal dominant type IV Ehlers-Danlos syndrome
Rattus norvegicus (Norway rat)
DOID:14756
  • vascular type Ehlers-Danlos syndrome
  • Aliases:
    • autosomal dominant type IV Ehlers-Danlos syndrome
Mus musculus (house mouse)
DOID:14757
  • Ehlers-Danlos syndrome hypermobility type
  • Aliases:
    • Ehlers-Danlos syndrome, type 3
    • type III Ehlers-Danlos syndrome
Mus musculus (house mouse)
DOID:0112195
  • spondyloperipheral dysplasia
  • Aliases:
    • spondyloperipheral dysplasia-short ulna syndrome
Rattus norvegicus (Norway rat)
DOID:0112281
  • spondyloepiphyseal dysplasia Stanescu type
  • Aliases:
    • SED Stanescu type
    • SEDSTN
Rattus norvegicus (Norway rat)
DOID:0080044
  • hypochondrogenesis
Rattus norvegicus (Norway rat)
DOID:0080028
  • spondyloepimetaphyseal dysplasia, Strudwick type
Rattus norvegicus (Norway rat)

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Last updated: December 9, 2024