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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 13626 - 13650 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0060870
  • isolated growth hormone deficiency
  • Aliases:
    • IGHD
    • congenital IGHD
    • congenital isolated GH deficiency
    • congenital isolated growth hormone deficiency
    • familial isolated growth hormone deficiency
    • non-acquired isolated growth hormone deficiency
Mus musculus (house mouse)
DOID:0060870
  • isolated growth hormone deficiency
  • Aliases:
    • IGHD
    • congenital IGHD
    • congenital isolated GH deficiency
    • congenital isolated growth hormone deficiency
    • familial isolated growth hormone deficiency
    • non-acquired isolated growth hormone deficiency
Drosophila melanogaster (fruit fly)
DOID:0060870
  • isolated growth hormone deficiency
  • Aliases:
    • IGHD
    • congenital IGHD
    • congenital isolated GH deficiency
    • congenital isolated growth hormone deficiency
    • familial isolated growth hormone deficiency
    • non-acquired isolated growth hormone deficiency
Homo sapiens (human)
DOID:0060870
  • isolated growth hormone deficiency
  • Aliases:
    • IGHD
    • congenital IGHD
    • congenital isolated GH deficiency
    • congenital isolated growth hormone deficiency
    • familial isolated growth hormone deficiency
    • non-acquired isolated growth hormone deficiency
Rattus norvegicus (Norway rat)
DOID:0060869
  • late-onset retinal degeneration
  • Aliases:
    • LORD
    • autosomal dominant late-onset retinal degeneration
Mus musculus (house mouse)
DOID:0060868
  • leukoencephalopathy with vanishing white matter
  • Aliases:
    • CACH
    • CACH/VWM
    • childhood ataxia with central nervous system hypomyelination
    • vanishing white matter leukodystrophy
Homo sapiens (human)
DOID:0060868
  • leukoencephalopathy with vanishing white matter
  • Aliases:
    • CACH
    • CACH/VWM
    • childhood ataxia with central nervous system hypomyelination
    • vanishing white matter leukodystrophy
Saccharomyces cerevisiae S288C
DOID:0060868
  • leukoencephalopathy with vanishing white matter
  • Aliases:
    • CACH
    • CACH/VWM
    • childhood ataxia with central nervous system hypomyelination
    • vanishing white matter leukodystrophy
Mus musculus (house mouse)
DOID:0060867
  • macrocephaly-autism syndrome
  • Aliases:
    • macrocephaly-intellectual disability-autism syndrome
Homo sapiens (human)
DOID:0060866
  • patterned macular dystrophy 1
  • Aliases:
    • MDPT1
    • butterfly-shaped pigmentary maculary dystrophy 1
Rattus norvegicus (Norway rat)
DOID:0060866
  • patterned macular dystrophy 1
  • Aliases:
    • MDPT1
    • butterfly-shaped pigmentary maculary dystrophy 1
Xenopus laevis (African clawed frog)
DOID:0060866
  • patterned macular dystrophy 1
  • Aliases:
    • MDPT1
    • butterfly-shaped pigmentary maculary dystrophy 1
Homo sapiens (human)
DOID:0060866
  • patterned macular dystrophy 1
  • Aliases:
    • MDPT1
    • butterfly-shaped pigmentary maculary dystrophy 1
Mus musculus (house mouse)
DOID:0060864
  • patterned macular dystrophy 2
  • Aliases:
    • MDPT2
    • butterfly-shaped pigmentary maculary dystrophy 2
Homo sapiens (human)
DOID:0060863
  • patterned macular dystrophy
  • Aliases:
    • patterned dystrophy of retinal pigment epithelium
Xenopus laevis (African clawed frog)
DOID:0060863
  • patterned macular dystrophy
  • Aliases:
    • patterned dystrophy of retinal pigment epithelium
Rattus norvegicus (Norway rat)
DOID:0060863
  • patterned macular dystrophy
  • Aliases:
    • patterned dystrophy of retinal pigment epithelium
Mus musculus (house mouse)
DOID:0060863
  • patterned macular dystrophy
  • Aliases:
    • patterned dystrophy of retinal pigment epithelium
Homo sapiens (human)
DOID:0060861
  • microphthalmia with limb anomalies
  • Aliases:
    • MLA
    • OAS
    • Waardenburg anophthalmia syndrome
    • anophthalmia-syndactyly syndrome
    • ophthalmoacromelic syndrome
Mus musculus (house mouse)
DOID:0060861
  • microphthalmia with limb anomalies
  • Aliases:
    • MLA
    • OAS
    • Waardenburg anophthalmia syndrome
    • anophthalmia-syndactyly syndrome
    • ophthalmoacromelic syndrome
Homo sapiens (human)
DOID:0060859
  • salmonellosis
  • Aliases:
    • Salmonella infection
Homo sapiens (human)
DOID:0060859
  • salmonellosis
  • Aliases:
    • Salmonella infection
Mus musculus (house mouse)
DOID:0060858
  • hypotonia-cystinuria syndrome
  • Aliases:
    • cystinuria with mitochondrial disease
Homo sapiens (human)
DOID:0060856
  • right atrial isomerism
  • Aliases:
    • Ivemark syndrome
    • asplenia with cardiovascular anomalies
Homo sapiens (human)
DOID:0060856
  • right atrial isomerism
  • Aliases:
    • Ivemark syndrome
    • asplenia with cardiovascular anomalies
Rattus norvegicus (Norway rat)
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Last updated: December 9, 2024