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 9701 - 9725 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:0110773
  • hereditary spastic paraplegia 2
  • Aliases:
    • SPG2
    • X-linked spastic paraplegia 2
    • spastic paraplegia type 2
Mus musculus (house mouse)
DOID:3210
  • Pelizaeus-Merzbacher disease
  • Aliases:
    • HLD1
    • Leukodystrophy, sudanophilic
    • PMD
    • Pelizaeus Merzbacher brain sclerosis
    • Pelizaeus-Merzbacher brain sclerosis
    • diffuse familial brain sclerosis
    • hypomyelinating leukodystrophy 1
    • sudanophilic leukodystrophy, Paelizeus-Merzbacher type
Mus musculus (house mouse)
DOID:0080734
  • Ehlers-Danlos syndrome kyphoscoliotic type 1
Mus musculus (house mouse)
DOID:0060601
  • alpha-2-plasmin inhibitor deficiency
  • Aliases:
    • antiplasmin defiency
    • plasmin inhibitor deficiency
Mus musculus (house mouse)
DOID:0111592
  • plasminogen deficiency type I
  • Aliases:
    • hypoplasminogenemia
Mus musculus (house mouse)
DOID:0090017
  • epidermolysis bullosa simplex with muscular dystrophy
  • Aliases:
    • epidermolysis bullosa simplex and limb-girdle muscular dystrophy
    • limb-girdle muscular dystrophy with epidermolysis bullosa simplex
Mus musculus (house mouse)
DOID:0060736
  • epidermolysis bullosa simplex Ogna type
  • Aliases:
    • EBS-O
    • EBS-Og
    • EBSOG
Mus musculus (house mouse)
DOID:0110285
  • autosomal recessive limb-girdle muscular dystrophy type 2Q
  • Aliases:
    • LGMD2Q
    • autosomal recessive limb-girdle muscular dystrophy due to plectin deficiency
    • muscular dystrophy, limb-girdle, type 2Q
Mus musculus (house mouse)
DOID:0111745
  • cerebellar ataxia type 43
  • Aliases:
    • SCA43
Caenorhabditis elegans
DOID:0110160
  • Charcot-Marie-Tooth disease axonal type 2T
  • Aliases:
    • AR-CMT2T
    • CMT2T
    • Charcot-Marie-Tooth neuropathy type 2T
    • autosomal recessive axonal Charcot-Marie-Tooth disease type 2T
Caenorhabditis elegans
DOID:0080288
  • spinocerebellar ataxia 46
Mus musculus (house mouse)
DOID:0080081
  • nonsyndromic congenital nail disorder 3
Mus musculus (house mouse)
DOID:0112303
  • spondylometaphyseal dysplasia with corneal dystrophy
  • Aliases:
    • SMDCD
Mus musculus (house mouse)
DOID:11729
  • Lyme disease
  • Aliases:
    • Bannwarth syndrome
    • Bannworth's syndrome
    • Lyme borreliosis
    • Neurological Lyme disease
    • lyme neuroborreliosis
    • neuroborreliosis
Mus musculus (house mouse)
DOID:14566
  • disease of cellular proliferation
  • Aliases:
    • cell process disease
    • neoplasm
Mus musculus (house mouse)
DOID:1247
  • blood coagulation disease
  • Aliases:
    • coagulation protein disease
    • postpartum coagulation defect
    • postpartum coagulation defect with delivery
Mus musculus (house mouse)
DOID:2615
  • papilloma
  • Aliases:
    • papillomatosis
Mus musculus (house mouse)
DOID:0080411
  • familial adenomatous polyposis 3
Caenorhabditis elegans
DOID:0110859
  • polycystic kidney disease 2
  • Aliases:
    • Apkd2
    • Pkd2
    • Polycystic Kidney Disease, Adult, Type II
Mus musculus (house mouse)
DOID:0050964
  • spinocerebellar ataxia type 14
Mus musculus (house mouse)
DOID:0110658
  • congenital myasthenic syndrome 15
  • Aliases:
    • CMS15
    • congenital myasthenic syndrome 15 without tubular aggregates
Caenorhabditis elegans
DOID:1508
  • candidiasis
  • Aliases:
    • Disseminated candidiasis
    • systemic candidiasis
Caenorhabditis elegans
DOID:0110637
  • muscular dystrophy-dystroglycanopathy type B6
  • Aliases:
    • MDC1D
    • MDDGB6
    • congenital muscular dystrophy LARGE-related
    • congenital muscular dystrophy type 1D
    • muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 6
    • muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6
Caenorhabditis elegans
DOID:0111242
  • congenital muscular dystrophy-dystroglycanopathy type A6
  • Aliases:
    • MDDGA6
    • Walker-Warburg syndrome or muscle-eye-brain disease, LARGE-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A6
Caenorhabditis elegans
DOID:0060653
  • lethal congenital contracture syndrome 3
  • Aliases:
    • Israeli Bedouin type B multiple contracture syndrome
Mus musculus (house mouse)

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Last updated: December 9, 2024