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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 226 - 250 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source ▲
DOID:0050461
  • aspartylglucosaminuria
  • Aliases:
    • aspartylglucosaminidase deficiency
    • aspartylglycosaminuria
    • glycosylasparaginase deficiency
Drosophila melanogaster (fruit fly)
DOID:0050461
  • aspartylglucosaminuria
  • Aliases:
    • aspartylglucosaminidase deficiency
    • aspartylglycosaminuria
    • glycosylasparaginase deficiency
Mus musculus (house mouse)
DOID:0050461
  • aspartylglucosaminuria
  • Aliases:
    • aspartylglucosaminidase deficiency
    • aspartylglycosaminuria
    • glycosylasparaginase deficiency
Caenorhabditis elegans
DOID:0050461
  • aspartylglucosaminuria
  • Aliases:
    • aspartylglucosaminidase deficiency
    • aspartylglycosaminuria
    • glycosylasparaginase deficiency
Rattus norvegicus (Norway rat)
DOID:0050462
  • Antley-Bixler syndrome with disordered steroidogenesis
  • Aliases:
    • trapezoidocephaly-synostosis syndrome
Mus musculus (house mouse)
DOID:0050462
  • Antley-Bixler syndrome with disordered steroidogenesis
  • Aliases:
    • trapezoidocephaly-synostosis syndrome
Homo sapiens (human)
DOID:0050463
  • campomelic dysplasia
  • Aliases:
    • Acampomelic Campomelic Dysplasia
Homo sapiens (human)
DOID:0050464
  • Farber lipogranulomatosis
  • Aliases:
    • Farber disease
    • N-laurylsphingosine deacylase deficiency
    • acid ceramidase deficiency
Caenorhabditis elegans
DOID:0050464
  • Farber lipogranulomatosis
  • Aliases:
    • Farber disease
    • N-laurylsphingosine deacylase deficiency
    • acid ceramidase deficiency
Mus musculus (house mouse)
DOID:0050464
  • Farber lipogranulomatosis
  • Aliases:
    • Farber disease
    • N-laurylsphingosine deacylase deficiency
    • acid ceramidase deficiency
Rattus norvegicus (Norway rat)
DOID:0050465
  • Muir-Torre syndrome
Homo sapiens (human)
DOID:0050465
  • Muir-Torre syndrome
Mus musculus (house mouse)
DOID:0050466
  • Loeys-Dietz syndrome
Rattus norvegicus (Norway rat)
DOID:0050466
  • Loeys-Dietz syndrome
Homo sapiens (human)
DOID:0050466
  • Loeys-Dietz syndrome
Mus musculus (house mouse)
DOID:0050466
  • Loeys-Dietz syndrome
Caenorhabditis elegans
DOID:0050467
  • erythrokeratodermia variabilis
  • Aliases:
    • Erythrokeratodermia Figurata Variabilis
    • Greither Disease
Mus musculus (house mouse)
DOID:0050469
  • Costello syndrome
  • Aliases:
    • FCS SYNDROME
    • Faciocutaneoskeletal Syndrome
Homo sapiens (human)
DOID:0050470
  • Donohue syndrome
  • Aliases:
    • Leprechaunism
Homo sapiens (human)
DOID:0050470
  • Donohue syndrome
  • Aliases:
    • Leprechaunism
Caenorhabditis elegans
DOID:0050470
  • Donohue syndrome
  • Aliases:
    • Leprechaunism
Mus musculus (house mouse)
DOID:0050470
  • Donohue syndrome
  • Aliases:
    • Leprechaunism
Drosophila melanogaster (fruit fly)
DOID:0050470
  • Donohue syndrome
  • Aliases:
    • Leprechaunism
Xenopus laevis (African clawed frog)
DOID:0050471
  • Carney complex
  • Aliases:
    • Carney Complex, Type 1
    • Carney Complex, Type 2
    • Carney Syndrome
    • Carney complex variant
    • LAMB Syndrome
    • NAME Syndrome
Homo sapiens (human)
DOID:0050473
  • Alstrom syndrome
Mus musculus (house mouse)
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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024