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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 7176 - 7200 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0060322
  • mastoiditis
Rattus norvegicus (Norway rat)
DOID:0111951
  • immunodeficiency 40
  • Aliases:
    • DOCK2 deficiency
    • IMD40
Mus musculus (house mouse)
DOID:8577
  • ulcerative colitis
  • Aliases:
    • Left-sided ulcerative colitis
Xenopus laevis (African clawed frog)
DOID:13207
  • proliferative diabetic retinopathy
  • Aliases:
    • PDR
Caenorhabditis elegans
DOID:0111625
  • ventriculomegaly - cystic kidney disease
  • Aliases:
    • VMCKD
    • congenital nephrosis-cerebral ventriculomegaly syndrome
    • cystic kidney disease with ventriculomegaly
    • ventriculomegaly with cystic kidney disease
Homo sapiens (human)
DOID:0060708
  • lymphoproliferative syndrome 2
  • Aliases:
    • CD27 deficiency
    • LPFS2
Homo sapiens (human)
DOID:0070247
  • autosomal dominant Emery-Dreifuss muscular dystrophy 2
  • Aliases:
    • EDMD2
    • EMD2
    • Emery-Dreifuss muscular dystrophy 2, autosomal dominant
    • Emery-Dreifuss muscular dystrophy, autosomal dominant
    • Hauptmann-Thannhauser muscular dystrophy
    • autosomal dominant limb-girdle muscular dystrophy type 1B
    • muscular dystrophy with early contractures and cardiomyopathy, autosomal dominant
    • scapuloilioperoneal atrophy with cardiopathy
Mus musculus (house mouse)
DOID:0050675
  • Birk-Barel syndrome
  • Aliases:
    • Birk-Barel mental retardation dysmorphism syndrome
Caenorhabditis elegans
DOID:0070379
  • developmental and epileptic encephalopathy 6B
  • Aliases:
    • DEE6B
Homo sapiens (human)
DOID:0110456
  • dilated cardiomyopathy 1R
  • Aliases:
    • CMD1R
Rattus norvegicus (Norway rat)
DOID:0110180
  • Charcot-Marie-Tooth disease axonal type 2CC
  • Aliases:
    • CMT2CC
    • Charcot-Marie-Tooth neuropathy type 2CC
Homo sapiens (human)
DOID:4450
  • renal cell carcinoma
  • Aliases:
    • RCC
    • adenocarcinoma of kidney
    • hypernephroma
Mus musculus (house mouse)
DOID:1168
  • familial hyperlipidemia
  • Aliases:
    • familial hyperlipoproteinemia
    • hyperlipemia
Danio rerio (zebrafish)
DOID:0060712
  • autosomal recessive congenital ichthyosis 4A
  • Aliases:
    • ARCI4A
    • ICR2B
    • ichthyosis congenita IIB
    • lamellar ichthyosis 2
Mus musculus (house mouse)
DOID:13948
  • bladder neck obstruction
  • Aliases:
    • Obstruction of bladder neck or vesicourethral orifice
Caenorhabditis elegans
DOID:1920
  • hyperuricemia
  • Aliases:
    • Blood urate raized
    • uricacidemia
Rattus norvegicus (Norway rat)
DOID:0070374
  • leukoencephalopathy with vanishing white matter 1
Homo sapiens (human)
DOID:0110284
  • autosomal recessive limb-girdle muscular dystrophy type 2L
  • Aliases:
    • LGMD2L
    • muscular dystrophy, limb-girdle, type 2L
Danio rerio (zebrafish)
DOID:0060686
  • autosomal dominant nocturnal frontal lobe epilepsy 5
  • Aliases:
    • ENFL5
    • nocturnal frontal lobe epilepsy 5
Homo sapiens (human)
DOID:8454
  • riboflavin deficiency
  • Aliases:
    • ariboflavinosis
    • vitamin B2 deficiency
Homo sapiens (human)
DOID:5773
  • oral submucous fibrosis
  • Aliases:
    • Oral cavity Submucous Fibrosis
    • Oral submucosal fibrosis
    • Oral submucosal fibrosis, including of tongue
Homo sapiens (human)
DOID:0060577
  • 3MC syndrome 3
Mus musculus (house mouse)
DOID:0080552
  • congenital disorder of glycosylation Ia
  • Aliases:
    • PMM2-congenital disorder of glycosylation
    • congenital disorder of glycosylation 1a
Saccharomyces cerevisiae S288C
DOID:999
  • hypereosinophilic syndrome
  • Aliases:
    • Eosinophilic leukocytosis
    • eosinophilia
Danio rerio (zebrafish)
DOID:0111042
  • glycogen storage disease IXa
  • Aliases:
    • GSD type 9A
    • GSD type IXa
    • GSD9A
    • glycogen storage disease type 9A
    • glycogen storage disease type IXa
    • glycogenosis type 9A
    • glycogenosis type IXa
Mus musculus (house mouse)
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Last updated: December 9, 2024