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 2426 - 2450 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0070035
  • autosomal dominant intellectual developmental disorder 5
  • Aliases:
    • MRD5
    • autosomal dominant mental retardation 5
    • autosomal dominant non-syndromic intellectual disability 5
Saccharomyces cerevisiae S288C
DOID:0060799
  • syndromic X-linked intellectual disability Lubs type
  • Aliases:
    • Lubs X-linked mental retardation syndrome
    • MECP2 duplication syndrome
    • MRXSL
    • X-linked intellectual disability-hypotonia-recurrent Infections syndrome
    • mental retardation, X-linked, syndromic, Lubs type
    • mental retardation, X-linked, with recurrent respiratory infections
Rattus norvegicus (Norway rat)
DOID:0081290
  • Antley-Bixler syndrome without disordered steroidogenesis
Mus musculus (house mouse)
DOID:2377
  • multiple sclerosis
  • Aliases:
    • Generalized multiple sclerosis
    • insular sclerosis
Drosophila melanogaster (fruit fly)
DOID:0110032
  • autosomal dominant Alport syndrome
Homo sapiens (human)
DOID:0110106
  • atrial heart septal defect 1
  • Aliases:
    • ASD1
    • atrial septal defect 1
Rattus norvegicus (Norway rat)
DOID:0110871
  • congenital stationary night blindness 2A
  • Aliases:
    • congenital stationary night blindness 2A X-linked
Mus musculus (house mouse)
DOID:0110272
  • cataract 40
  • Aliases:
    • CTRCT40
    • cataract 40 X-linked
    • cataract 40 with or without microcornea
Homo sapiens (human)
DOID:0110739
  • neurodegeneration with brain iron accumulation 5
  • Aliases:
    • BPAN
    • Beta-Propeller Protein-Associated Neurodegeneration
    • NBIA5
    • SENDA
    • Static Encephalopathy Of Childhood With Neurodegeneration In Adulthood
Rattus norvegicus (Norway rat)
DOID:0110977
  • brachydactyly type A1C
  • Aliases:
    • BDA1C
Mus musculus (house mouse)
DOID:2957
  • pulmonary tuberculosis
Danio rerio (zebrafish)
DOID:0060475
  • myoclonic-atonic epilepsy
  • Aliases:
    • EEOC
    • childhood onset epileptic encephalopathy
Homo sapiens (human)
DOID:14069
  • cerebral malaria
  • Aliases:
    • Malarial encephalitis
Homo sapiens (human)
DOID:0050866
  • oral squamous cell carcinoma
  • Aliases:
    • mouth squamous cell carcinoma
Drosophila melanogaster (fruit fly)
DOID:0060001
  • withdrawal disorder
Mus musculus (house mouse)
DOID:1245
  • vulva cancer
  • Aliases:
    • Ca vulva
    • Vulvar tumor
    • malignant Vulvar tumor
    • malignant neoplasm of vulva
    • malignant tumor of vulva
    • neoplasm of vulva
    • vulval cancer
    • vulval neoplasm
    • vulvar neoplasm
Mus musculus (house mouse)
DOID:75
  • lymphatic system disease
  • Aliases:
    • Lymphangiopathy
    • Lymphatic disease
    • disease of lympoid system
    • disorder of lymph node and lymphatics
    • disorder of lymphatic system
    • disorder of lymphoid system
    • lymphatic disorder
    • lympoid system disease
Rattus norvegicus (Norway rat)
DOID:0050637
  • Finnish type amyloidosis
  • Aliases:
    • AGel amyloidosis
    • AMYLOIDOSIS, MERETOJA TYPE
    • Lattice corneal dystrophy type II
    • gelsolin amyloidosis
Homo sapiens (human)
DOID:9428
  • intracranial hypertension
  • Aliases:
    • Raised intracranial pressure
Homo sapiens (human)
DOID:850
  • lung disease
Drosophila melanogaster (fruit fly)
DOID:12306
  • vitiligo
Caenorhabditis elegans
DOID:0060224
  • atrial fibrillation
  • Aliases:
    • A-fib
    • AFib
Saccharomyces cerevisiae S288C
DOID:9246
  • cerebral amyloid angiopathy
  • Aliases:
    • Cerebral Hemorrhage, Hereditary, with Amyloidosis
    • Hereditary Cerebral Hemorrhage with Amyloidosis
Rattus norvegicus (Norway rat)
DOID:9675
  • pulmonary emphysema
Saccharomyces cerevisiae S288C
DOID:0111241
  • congenital muscular dystrophy-dystroglycanopathy type A5
  • Aliases:
    • MDDGA5
    • Walker-Warburg syndrome or muscle-eye-brain disease, FKRP-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5
Xenopus tropicalis (tropical clawed frog)

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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