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 10201 - 10225 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:4667
  • kyphosis
  • Aliases:
    • Kyphosis deformity of spine
Mus musculus (house mouse)
DOID:0050981
  • spinocerebellar ataxia type 34
Mus musculus (house mouse)
DOID:2566
  • corneal dystrophy
Mus musculus (house mouse)
DOID:0080625
  • severe congenital neutropenia 1
Mus musculus (house mouse)
DOID:5339
  • cyclic hematopoiesis
  • Aliases:
    • Cyclic neutropenia
    • Cyclical neutropenia
    • Neutropenia, periodic
    • cyclic agranulocytosis
Mus musculus (house mouse)
DOID:2562
  • suppurative periapical periodontitis
  • Aliases:
    • Apical abscess
    • Dentoalveolar abscess
    • Periapical abscess
    • Suppurative apical periodontitis
Mus musculus (house mouse)
DOID:0080178
  • mucositis
Mus musculus (house mouse)
DOID:0060479
  • Shwachman-Diamond syndrome
  • Aliases:
    • Shwachman syndrome
    • Shwachman-Bodian-Diamond syndrome
    • Shwachman-Diamond type metaphyseal dysplasia
    • pancreatic insufficiency and bone marrow dysfunction
Mus musculus (house mouse)
DOID:0081228
  • autosomal recessive intellectual developmental disorder 67
Mus musculus (house mouse)
DOID:9406
  • hypopituitarism
  • Aliases:
    • Pituitary insufficiency
    • pituitary hormone deficiency
Mus musculus (house mouse)
DOID:0060801
  • MEHMO syndrome
  • Aliases:
    • MRXS20
    • MRXS25
    • X-linked intellectual disability-epileptic seizures-hypogenitalism-microcephaly-obesity syndrome
    • mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity
    • syndromic X-linked mental retardation 20
    • syndromic X-linked mental retardation 25
Mus musculus (house mouse)
DOID:4194
  • glucose metabolism disease
  • Aliases:
    • disorder of glucose metabolism
Mus musculus (house mouse)
DOID:0070367
  • leukoencephalopathy with vanishing white matter 5
  • Aliases:
    • Cree leukoencephalopathy
Mus musculus (house mouse)
DOID:0070371
  • leukoencephalopathy with vanishing white matter 4
Mus musculus (house mouse)
DOID:0060868
  • leukoencephalopathy with vanishing white matter
  • Aliases:
    • CACH
    • CACH/VWM
    • childhood ataxia with central nervous system hypomyelination
    • vanishing white matter leukodystrophy
Mus musculus (house mouse)
DOID:0090060
  • Wolcott-Rallison syndrome
Rattus norvegicus (Norway rat)
DOID:0090060
  • Wolcott-Rallison syndrome
Mus musculus (house mouse)
DOID:0060352
  • Kleefstra syndrome 1
  • Aliases:
    • 9q subtelomeric deletion syndrome
    • 9q-syndrome
    • 9q34 deletion syndrome
Mus musculus (house mouse)
DOID:0080597
  • Kleefstra syndrome
Mus musculus (house mouse)
DOID:0080338
  • familial erythrocytosis 3
  • Aliases:
    • ECYT3
Mus musculus (house mouse)
DOID:13133
  • HELLP syndrome
Drosophila melanogaster (fruit fly)
DOID:0060560
  • lethal congenital contracture syndrome 2
  • Aliases:
    • LCCS2
    • multiple contracture syndrome, Israeli-Bedouin type
Drosophila melanogaster (fruit fly)
DOID:0060210
  • amyotrophic lateral sclerosis type 19
  • Aliases:
    • ALS19
    • amyotrophic lateral sclerosis 19
Drosophila melanogaster (fruit fly)
DOID:0080679
  • neuronal intestinal dysplasia type A
Drosophila melanogaster (fruit fly)
DOID:3443
  • mammary Paget's disease
  • Aliases:
    • Paget cell neoplasm
    • Paget's disease
    • Paget's disease of the breast
    • mammary Paget disease
Drosophila melanogaster (fruit fly)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024