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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 8101 - 8125 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0111664
  • ectodermal dysplasia 1
  • Aliases:
    • CST syndrome
    • Christ-Siemens-Touraine syndrome
    • ED1
    • HED1
    • X-linked anhidrotic ectodermal dysplasia
    • XHED
    • XLHED
    • ectodermal dysplasia 1, anhidrotic
    • ectodermal dysplasia 1, hypohidrotic, X-linked
    • ectodermal dysplasia 1, hypohidrotic/hair/tooth type, X-linked
    • hypohidrotic ectodermal dysplasia, X-Linked
Homo sapiens (human)
DOID:0111664
  • ectodermal dysplasia 1
  • Aliases:
    • CST syndrome
    • Christ-Siemens-Touraine syndrome
    • ED1
    • HED1
    • X-linked anhidrotic ectodermal dysplasia
    • XHED
    • XLHED
    • ectodermal dysplasia 1, anhidrotic
    • ectodermal dysplasia 1, hypohidrotic, X-linked
    • ectodermal dysplasia 1, hypohidrotic/hair/tooth type, X-linked
    • hypohidrotic ectodermal dysplasia, X-Linked
Drosophila melanogaster (fruit fly)
DOID:0111664
  • ectodermal dysplasia 1
  • Aliases:
    • CST syndrome
    • Christ-Siemens-Touraine syndrome
    • ED1
    • HED1
    • X-linked anhidrotic ectodermal dysplasia
    • XHED
    • XLHED
    • ectodermal dysplasia 1, anhidrotic
    • ectodermal dysplasia 1, hypohidrotic, X-linked
    • ectodermal dysplasia 1, hypohidrotic/hair/tooth type, X-linked
    • hypohidrotic ectodermal dysplasia, X-Linked
Mus musculus (house mouse)
DOID:0111663
  • ectodermal dysplasia 10A
  • Aliases:
    • ECTD10A
    • ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant
Homo sapiens (human)
DOID:0111663
  • ectodermal dysplasia 10A
  • Aliases:
    • ECTD10A
    • ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant
Mus musculus (house mouse)
DOID:0111662
  • ectodermal dysplasia 14
  • Aliases:
    • ECTN14
    • ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis
Homo sapiens (human)
DOID:0111662
  • ectodermal dysplasia 14
  • Aliases:
    • ECTN14
    • ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis
Mus musculus (house mouse)
DOID:0111651
  • ectodermal dysplasia 15
  • Aliases:
    • ECTD15
    • ectodermal dysplasia 15, hypohidrotic/hair type
Mus musculus (house mouse)
DOID:0111651
  • ectodermal dysplasia 15
  • Aliases:
    • ECTD15
    • ectodermal dysplasia 15, hypohidrotic/hair type
Caenorhabditis elegans
DOID:0111651
  • ectodermal dysplasia 15
  • Aliases:
    • ECTD15
    • ectodermal dysplasia 15, hypohidrotic/hair type
Homo sapiens (human)
DOID:0111650
  • ectodermal dysplasia 13
  • Aliases:
    • ECTD13
    • ectodermal dysplasia 13, hair/tooth type
Xenopus laevis (African clawed frog)
DOID:0111650
  • ectodermal dysplasia 13
  • Aliases:
    • ECTD13
    • ectodermal dysplasia 13, hair/tooth type
Mus musculus (house mouse)
DOID:0111650
  • ectodermal dysplasia 13
  • Aliases:
    • ECTD13
    • ectodermal dysplasia 13, hair/tooth type
Homo sapiens (human)
DOID:0111650
  • ectodermal dysplasia 13
  • Aliases:
    • ECTD13
    • ectodermal dysplasia 13, hair/tooth type
Rattus norvegicus (Norway rat)
DOID:0111649
  • ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome
  • Aliases:
    • EEM syndrome
    • EEMS
    • ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome
Danio rerio (zebrafish)
DOID:0111649
  • ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome
  • Aliases:
    • EEM syndrome
    • EEMS
    • ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome
Homo sapiens (human)
DOID:0111649
  • ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome
  • Aliases:
    • EEM syndrome
    • EEMS
    • ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome
Mus musculus (house mouse)
DOID:0111648
  • ectopia lentis with ectopia of pupil
  • Aliases:
    • ectopia lentis et pupillae
Rattus norvegicus (Norway rat)
DOID:0111648
  • ectopia lentis with ectopia of pupil
  • Aliases:
    • ectopia lentis et pupillae
Homo sapiens (human)
DOID:0111648
  • ectopia lentis with ectopia of pupil
  • Aliases:
    • ectopia lentis et pupillae
Mus musculus (house mouse)
DOID:0111647
  • Schopf-Schulz-Passarge syndrome
  • Aliases:
    • SSPS
    • eccrine tumors-ectodermal dysplasia
    • keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome
    • palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome
    • palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome
Caenorhabditis elegans
DOID:0111647
  • Schopf-Schulz-Passarge syndrome
  • Aliases:
    • SSPS
    • eccrine tumors-ectodermal dysplasia
    • keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome
    • palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome
    • palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome
Homo sapiens (human)
DOID:0111647
  • Schopf-Schulz-Passarge syndrome
  • Aliases:
    • SSPS
    • eccrine tumors-ectodermal dysplasia
    • keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome
    • palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome
    • palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome
Mus musculus (house mouse)
DOID:0111646
  • congenital lactase deficiency
  • Aliases:
    • CLD
    • congenital alactasia
    • congenital alactasia syndrome
    • congenital lactose intolerance
    • congenital lactose malabsorption
    • disaccharide intolerance II
Homo sapiens (human)
DOID:0111644
  • autosomal recessive nonsyndromic deafness 110
  • Aliases:
    • DFNB110
    • autosomal recessive deafness 110
Mus musculus (house mouse)
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Last updated: December 9, 2024