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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 15801 - 15825 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:0080630
  • B-lymphoblastic leukemia/lymphoma
  • Aliases:
    • B lymphoblastic leukemia/lymphoma
    • B-ALL
    • precursor B lymphoblastic lymphoma/leukemia
Mus musculus (house mouse)
DOID:0080630
  • B-lymphoblastic leukemia/lymphoma
  • Aliases:
    • B lymphoblastic leukemia/lymphoma
    • B-ALL
    • precursor B lymphoblastic lymphoma/leukemia
Caenorhabditis elegans
DOID:707
  • B-cell lymphoma
  • Aliases:
    • B-cell lymphocytic neoplasm
Saccharomyces cerevisiae S288C
DOID:707
  • B-cell lymphoma
  • Aliases:
    • B-cell lymphocytic neoplasm
Mus musculus (house mouse)
DOID:707
  • B-cell lymphoma
  • Aliases:
    • B-cell lymphocytic neoplasm
Homo sapiens (human)
DOID:707
  • B-cell lymphoma
  • Aliases:
    • B-cell lymphocytic neoplasm
Drosophila melanogaster (fruit fly)
DOID:707
  • B-cell lymphoma
  • Aliases:
    • B-cell lymphocytic neoplasm
Rattus norvegicus (Norway rat)
DOID:2115
  • B cell deficiency
  • Aliases:
    • B cell (antibody) deficiencies
    • Immunoglobulin heavy chain deficiency
    • immunoglobulin heavy chain deletion
Mus musculus (house mouse)
DOID:2115
  • B cell deficiency
  • Aliases:
    • B cell (antibody) deficiencies
    • Immunoglobulin heavy chain deficiency
    • immunoglobulin heavy chain deletion
Homo sapiens (human)
DOID:14686
  • Axenfeld-Rieger syndrome
  • Aliases:
    • Anomaly, Rieger's
    • Axenfeld syndrome
    • RGS - Rieger syndrome
    • Rieger's anomaly
Homo sapiens (human)
DOID:0110122
  • Axenfeld-Rieger syndrome type 3
  • Aliases:
    • Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss
    • RIEG3
    • Rieger syndrome type 3
    • anterior chamber cleavage syndrome
    • anterior segment mesenchymal dysgenesis
Mus musculus (house mouse)
DOID:0110122
  • Axenfeld-Rieger syndrome type 3
  • Aliases:
    • Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss
    • RIEG3
    • Rieger syndrome type 3
    • anterior chamber cleavage syndrome
    • anterior segment mesenchymal dysgenesis
Homo sapiens (human)
DOID:0110122
  • Axenfeld-Rieger syndrome type 3
  • Aliases:
    • Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss
    • RIEG3
    • Rieger syndrome type 3
    • anterior chamber cleavage syndrome
    • anterior segment mesenchymal dysgenesis
Drosophila melanogaster (fruit fly)
DOID:0110122
  • Axenfeld-Rieger syndrome type 3
  • Aliases:
    • Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss
    • RIEG3
    • Rieger syndrome type 3
    • anterior chamber cleavage syndrome
    • anterior segment mesenchymal dysgenesis
Caenorhabditis elegans
DOID:0110120
  • Axenfeld-Rieger syndrome type 1
  • Aliases:
    • RIEG1
    • Rieger syndrome type 1
Homo sapiens (human)
DOID:0050432
  • Asperger syndrome
Homo sapiens (human)
DOID:0050432
  • Asperger syndrome
Drosophila melanogaster (fruit fly)
DOID:0050647
  • Arts syndrome
  • Aliases:
    • ARTS
    • Lethal ataxia with deafness and optic atrophy
    • MRXS18
    • MRXSARTS
    • fatal X-linked ataxia with deafness and loss of vision
    • syndromic X-linked mental retardation 18
    • syndromic X-linked mental retardation Arts type
Mus musculus (house mouse)
DOID:0050647
  • Arts syndrome
  • Aliases:
    • ARTS
    • Lethal ataxia with deafness and optic atrophy
    • MRXS18
    • MRXSARTS
    • fatal X-linked ataxia with deafness and loss of vision
    • syndromic X-linked mental retardation 18
    • syndromic X-linked mental retardation Arts type
Homo sapiens (human)
DOID:0070062
  • Arboleda-Tham syndrome
  • Aliases:
    • ARTHS
    • MRD32
    • autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
    • autosomal dominant mental retardation 32
    • autosomal dominant non-syndromic intellectual disability 32
Homo sapiens (human)
DOID:0070062
  • Arboleda-Tham syndrome
  • Aliases:
    • ARTHS
    • MRD32
    • autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
    • autosomal dominant mental retardation 32
    • autosomal dominant non-syndromic intellectual disability 32
Drosophila melanogaster (fruit fly)
DOID:0081289
  • Antley-Bixler syndrome
  • Aliases:
    • Antley Bixler syndrome
    • Antley and Bixler's syndrome
Danio rerio (zebrafish)
DOID:0081289
  • Antley-Bixler syndrome
  • Aliases:
    • Antley Bixler syndrome
    • Antley and Bixler's syndrome
Mus musculus (house mouse)
DOID:0081289
  • Antley-Bixler syndrome
  • Aliases:
    • Antley Bixler syndrome
    • Antley and Bixler's syndrome
Homo sapiens (human)
DOID:0081289
  • Antley-Bixler syndrome
  • Aliases:
    • Antley Bixler syndrome
    • Antley and Bixler's syndrome
Drosophila melanogaster (fruit fly)
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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: August 19, 2024