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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 6201 - 6225 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:0080528
  • bronchiectasis 3
Mus musculus (house mouse)
DOID:10300
  • Raynaud disease
  • Aliases:
    • Raynaud's disease
    • Raynaud's syndrome
Homo sapiens (human)
DOID:9675
  • pulmonary emphysema
Homo sapiens (human)
DOID:0111066
  • congenital bile acid synthesis defect 5
  • Aliases:
    • CBAS5
Mus musculus (house mouse)
DOID:0090110
  • immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome
  • Aliases:
    • Autoimmune enteropathy type 1
    • DMSD
    • IDDM-secretory diarrhea syndrome
    • IPEX
    • X-linked autoimmunity-allergic dysregulation syndrome
    • XLAAD
    • XPID
    • autoimmunity-immunodeficiency syndrome, X-linked
    • diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea
    • diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked
    • immunodeficiency, polyendocrinopathy, and enteropathy, X-linked
    • immunodysregulation, polyendocrinopathy, and enteropathy, X-Linked
Homo sapiens (human)
DOID:12986
  • leukostasis
Drosophila melanogaster (fruit fly)
DOID:14705
  • Pfeiffer syndrome
  • Aliases:
    • acrocephalosyndactylia type V
Danio rerio (zebrafish)
DOID:0110276
  • autosomal recessive limb-girdle muscular dystrophy type 2B
  • Aliases:
    • LGMD2B
    • LGMD3
    • limb-girdle muscular dystrophy due to dysferlin deficiency
    • limb-girdle muscular dystrophy type 3
Mus musculus (house mouse)
DOID:0060224
  • atrial fibrillation
  • Aliases:
    • A-fib
    • AFib
Xenopus tropicalis (tropical clawed frog)
DOID:631
  • fibromyalgia
Rattus norvegicus (Norway rat)
DOID:0110820
  • hereditary spastic paraplegia 75
  • Aliases:
    • SPG75
    • autosomal recessive spastic paraplegia 75
    • autosomal recessive spastic paraplegia type 75
Rattus norvegicus (Norway rat)
DOID:0050912
  • colon adenoma
Mus musculus (house mouse)
DOID:10223
  • dermatomyositis
  • Aliases:
    • Polymyositis with skin involvement
    • dermatopolymyositis
Rattus norvegicus (Norway rat)
DOID:0050328
  • congenital hypothyroidism
Homo sapiens (human)
DOID:0081225
  • autosomal recessive intellectual developmental disorder 64
Homo sapiens (human)
DOID:10591
  • pre-eclampsia
  • Aliases:
    • gestational hypertension
    • hypertension induced by pregnancy
    • pre-eclamptic toxaemia
    • preeclampsia
    • preeclampsia/eclampsia
    • pregnancy associated hypertension
    • pregnancy toxemia
    • proteinuric hypertension of pregnancy
    • toxaemia of pregnancy
Xenopus tropicalis (tropical clawed frog)
DOID:11870
  • Pick's disease
  • Aliases:
    • Dementia in Pick's disease
    • LOBAR ATROPHY OF BRAIN
    • PICK DISEASE OF BRAIN
    • Pick disease
Rattus norvegicus (Norway rat)
DOID:0080685
  • aortic dissection
Rattus norvegicus (Norway rat)
DOID:10787
  • premature menopause
  • Aliases:
    • Menopause - premature
    • Menopause praecox
Saccharomyces cerevisiae S288C
DOID:0110313
  • hypertrophic cardiomyopathy 7
  • Aliases:
    • CMH7
    • cardiomyopathy, familial hypertrophic 7
Rattus norvegicus (Norway rat)
DOID:0070205
  • familial partial lipodystrophy type 4
  • Aliases:
    • FPLD4
    • PLIN1-related FPLD
    • PLIN1-related familial partial lipodystrophy
    • familial partial lipodystrophy associated with PLIN1 mutations
Homo sapiens (human)
DOID:0090001
  • Fraser syndrome
  • Aliases:
    • cryptophthalmos with other malformations
Mus musculus (house mouse)
DOID:7998
  • hyperthyroidism
  • Aliases:
    • overactive thyroid
Xenopus tropicalis (tropical clawed frog)
DOID:0050763
  • ARC syndrome
  • Aliases:
    • ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS
    • Arthrogryposis, renal dysfunction and cholestasis (ARC) syndrome
    • Arthrogryposis-renal dysfunction-cholestasis
Homo sapiens (human)
DOID:13372
  • alpha 1-antitrypsin deficiency
  • Aliases:
    • AAT deficiency
Rattus norvegicus (Norway rat)
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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