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 4551 - 4575 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0070184
  • spermatogenic failure 16
  • Aliases:
    • SPGF16
    • acephalic spermatozoa syndrome
Mus musculus (house mouse)
DOID:11204
  • allergic conjunctivitis
Mus musculus (house mouse)
DOID:0081113
  • Baraitser-Winter syndrome 2
Mus musculus (house mouse)
DOID:0111552
  • scapuloperoneal spinal muscular atrophy
  • Aliases:
    • SPSMA
    • neurogenic scapuloperoneal amyotrophy, New England type
    • scapuloperoneal neuronopathy
Mus musculus (house mouse)
DOID:809
  • cocaine abuse
Mus musculus (house mouse)
DOID:0060894
  • early-onset Parkinson's disease
  • Aliases:
    • early-onset Parkinson disease
Mus musculus (house mouse)
DOID:0060967
  • dystonia 22, adult-onset
Mus musculus (house mouse)
DOID:0060040
  • pervasive developmental disorder
  • Aliases:
    • Pervasive Child Development Disorders
    • pervasive development disorder
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:2738
  • pseudoxanthoma elasticum
  • Aliases:
    • Gronblad-Strandberg syndrome
Mus musculus (house mouse)
DOID:0080059
  • autosomal recessive spinocerebellar ataxia 7
  • Aliases:
    • SCAR7
Mus musculus (house mouse)
DOID:0111578
  • Gillespie syndrome
  • Aliases:
    • GLSP
    • aniridia, cerebellar ataxia and mental deficiency
    • aniridia-cerebellar ataxia-intellectual disability syndrome
Mus musculus (house mouse)
DOID:2228
  • thrombocytosis
  • Aliases:
    • Thrombocythaemia
Mus musculus (house mouse)
DOID:0111526
  • Mullerian aplasia and hyperandrogenism
  • Aliases:
    • Mullerian duct failure and hyperandrogenism
    • WNT4 deficiency
Mus musculus (house mouse)
DOID:0050955
  • spinocerebellar ataxia type 2
Mus musculus (house mouse)
DOID:8805
  • intermediate coronary syndrome
  • Aliases:
    • Angina at rest
    • Anginal chest pain at rest
    • Impending infarction
    • Preinfarction angina
    • Unstable angina
    • Worsening angina
Mus musculus (house mouse)
DOID:0060900
  • Parkinson's disease 14
  • Aliases:
    • Dystonia-Parkinsonism Adult-Onset
    • autosomal recessive Parkinson disease 14
    • autosomal recessive Parkinson's disease 14
Mus musculus (house mouse)
DOID:0060686
  • autosomal dominant nocturnal frontal lobe epilepsy 5
  • Aliases:
    • ENFL5
    • nocturnal frontal lobe epilepsy 5
Mus musculus (house mouse)
DOID:0050155
  • sensory system disease
Mus musculus (house mouse)
DOID:12804
  • mucopolysaccharidosis IV
  • Aliases:
    • Mucopolysaccharidosis, MPS-IV
    • deficiency of N-acetylgalactosamine-6-sulphatase
    • deficiency of chondroitinsulphatase
    • galactosamine-6-sulfatase deficiency
Mus musculus (house mouse)
DOID:13533
  • osteopetrosis
  • Aliases:
    • Albers-Schonberg disease
    • marble bone
Mus musculus (house mouse)
DOID:1070
  • primary open angle glaucoma
  • Aliases:
    • chronic simple glaucoma
Mus musculus (house mouse)
DOID:2156
  • ovarian germ cell cancer
  • Aliases:
    • germ cell neoplasm of Ovary
    • germ cell tumor of ovary
Mus musculus (house mouse)
DOID:0081366
  • Paget's disease of bone 3
  • Aliases:
    • Paget disease of bone-3
Mus musculus (house mouse)
DOID:1891
  • optic nerve disease
  • Aliases:
    • disorder of the second nerve
    • optic nerve disorder
    • optic neuropathy
Mus musculus (house mouse)

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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