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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 13401 - 13425 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▼
DOID:0070098
  • oculocutaneous albinism type IV
  • Aliases:
    • OCA4
Mus musculus (house mouse)
DOID:0070097
  • oculocutaneous albinism type III
  • Aliases:
    • OCA3
    • Rufous Oculocutaneous Albinism
Mus musculus (house mouse)
DOID:0070097
  • oculocutaneous albinism type III
  • Aliases:
    • OCA3
    • Rufous Oculocutaneous Albinism
Homo sapiens (human)
DOID:0070097
  • oculocutaneous albinism type III
  • Aliases:
    • OCA3
    • Rufous Oculocutaneous Albinism
Caenorhabditis elegans
DOID:0070096
  • oculocutaneous albinism type II
  • Aliases:
    • OCA2
    • Oculocutaneous Albinism, Tyrosinase-Positive
Homo sapiens (human)
DOID:0070096
  • oculocutaneous albinism type II
  • Aliases:
    • OCA2
    • Oculocutaneous Albinism, Tyrosinase-Positive
Mus musculus (house mouse)
DOID:0070095
  • oculocutaneous albinism type IB
  • Aliases:
    • Albinism, Yellow Mutant Type
    • OCA1B
Mus musculus (house mouse)
DOID:0070095
  • oculocutaneous albinism type IB
  • Aliases:
    • Albinism, Yellow Mutant Type
    • OCA1B
Caenorhabditis elegans
DOID:0070095
  • oculocutaneous albinism type IB
  • Aliases:
    • Albinism, Yellow Mutant Type
    • OCA1B
Homo sapiens (human)
DOID:0070094
  • oculocutaneous albinism type IA
  • Aliases:
    • OCA1A
    • Oculocutaneous Albinism, Tyrosinase-Negative
Caenorhabditis elegans
DOID:0070094
  • oculocutaneous albinism type IA
  • Aliases:
    • OCA1A
    • Oculocutaneous Albinism, Tyrosinase-Negative
Mus musculus (house mouse)
DOID:0070094
  • oculocutaneous albinism type IA
  • Aliases:
    • OCA1A
    • Oculocutaneous Albinism, Tyrosinase-Negative
Homo sapiens (human)
DOID:0070093
  • schizophrenia 18
  • Aliases:
    • Chromosome 7q36.3 Duplication Syndrome, 362-Kb
    • SCZD18
Mus musculus (house mouse)
DOID:0070093
  • schizophrenia 18
  • Aliases:
    • Chromosome 7q36.3 Duplication Syndrome, 362-Kb
    • SCZD18
Homo sapiens (human)
DOID:0070093
  • schizophrenia 18
  • Aliases:
    • Chromosome 7q36.3 Duplication Syndrome, 362-Kb
    • SCZD18
Rattus norvegicus (Norway rat)
DOID:0070093
  • schizophrenia 18
  • Aliases:
    • Chromosome 7q36.3 Duplication Syndrome, 362-Kb
    • SCZD18
Caenorhabditis elegans
DOID:0070091
  • schizophrenia 15
  • Aliases:
    • SCZD15
Mus musculus (house mouse)
DOID:0070082
  • schizophrenia 6
  • Aliases:
    • SCZD6
Drosophila melanogaster (fruit fly)
DOID:0070082
  • schizophrenia 6
  • Aliases:
    • SCZD6
Homo sapiens (human)
DOID:0070074
  • autosomal dominant intellectual developmental disorder 44
  • Aliases:
    • MRD44
    • autosomal dominant intellectual developmental disorder 44 with microcephaly
    • autosomal dominant mental retardation 44
    • autosomal dominant non-syndromic intellectual disability 44
Homo sapiens (human)
DOID:0070074
  • autosomal dominant intellectual developmental disorder 44
  • Aliases:
    • MRD44
    • autosomal dominant intellectual developmental disorder 44 with microcephaly
    • autosomal dominant mental retardation 44
    • autosomal dominant non-syndromic intellectual disability 44
Mus musculus (house mouse)
DOID:0070073
  • autosomal dominant intellectual developmental disorder 43
  • Aliases:
    • MRD43
    • autosomal dominant mental retardation 43
    • autosomal dominant non-syndromic intellectual disability 43
Rattus norvegicus (Norway rat)
DOID:0070073
  • autosomal dominant intellectual developmental disorder 43
  • Aliases:
    • MRD43
    • autosomal dominant mental retardation 43
    • autosomal dominant non-syndromic intellectual disability 43
Mus musculus (house mouse)
DOID:0070073
  • autosomal dominant intellectual developmental disorder 43
  • Aliases:
    • MRD43
    • autosomal dominant mental retardation 43
    • autosomal dominant non-syndromic intellectual disability 43
Homo sapiens (human)
DOID:0070072
  • autosomal dominant intellectual developmental disorder 42
  • Aliases:
    • MRD42
    • autosomal dominant mental retardation 42
    • autosomal dominant non-syndromic intellectual disability 42
Mus musculus (house mouse)
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Last updated: December 9, 2024