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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 9951 - 9975 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0080268
  • autosomal dominant nonsyndromic deafness 72
Homo sapiens (human)
DOID:3713
  • ovary adenocarcinoma
  • Aliases:
    • Ovarian adenocarcinoma
    • ovarian adenoacanthoma
Homo sapiens (human)
DOID:14089
  • root caries
  • Aliases:
    • Cementum caries
    • Dental caries of root surface
Homo sapiens (human)
DOID:0050860
  • colorectal adenoma
Homo sapiens (human)
DOID:0070029
  • ITM2B-related cerebral amyloid angiopathy 1
  • Aliases:
    • Cerebral Amyloid Angiopathy, British Type
    • FBD
    • Familial British Dementia
    • Presenile Dementia with Spastic Ataxia
Homo sapiens (human)
DOID:5522
  • basaloid squamous cell carcinoma
  • Aliases:
    • Basaloid carcinoma
Homo sapiens (human)
DOID:0081290
  • Antley-Bixler syndrome without disordered steroidogenesis
Homo sapiens (human)
DOID:0080079
  • nonsyndromic congenital nail disorder 1
  • Aliases:
    • nonsyndromic congenital nail disorder 10
    • twenty-nail dystrophy
Homo sapiens (human)
DOID:0080046
  • Stickler syndrome
Homo sapiens (human)
DOID:0060546
  • Hermansky-Pudlak syndrome 8
Homo sapiens (human)
DOID:0080589
  • Klippel-Feil syndrome 1
Homo sapiens (human)
DOID:0070037
  • autosomal dominant intellectual developmental disorder 7
  • Aliases:
    • DYRK1A syndrome
    • MRD7
    • autosomal dominant mental retardation 7
    • autosomal dominant non-syndromic intellectual disability 7
Homo sapiens (human)
DOID:0111198
  • autosomal dominant distal hereditary motor neuronopathy
  • Aliases:
    • autosomal dominant dHMN
    • autosomal dominant distal hereditary motor neuropathy
    • autosomal dominant distal spinal muscular atrophy
Homo sapiens (human)
DOID:2810
  • middle lobe syndrome
Homo sapiens (human)
DOID:9733
  • renal tuberculosis
  • Aliases:
    • Tuberculosis of kidney
Homo sapiens (human)
DOID:0110674
  • congenital myasthenic syndrome 17
  • Aliases:
    • CMS17
Homo sapiens (human)
DOID:11702
  • dysgammaglobulinemia
Homo sapiens (human)
DOID:5374
  • pilomatrixoma
  • Aliases:
    • Pilomatricoma
    • benign pilomatricoma
Homo sapiens (human)
DOID:11656
  • cicatricial pemphigoid
  • Aliases:
    • Cicatricial pemphigoid with ocular involvement
    • Ocular pemphigoid
    • benign mucous membrane pemphigoid
    • benign mucous membrane pemphigoid with ocular involvement
    • ocular pemphigus
Homo sapiens (human)
DOID:0060718
  • autosomal recessive congenital ichthyosis 9
  • Aliases:
    • ARCI9
Homo sapiens (human)
DOID:0111461
  • cardiofaciocutaneous syndrome 2
  • Aliases:
    • CFC2
Homo sapiens (human)
DOID:0060823
  • syndromic X-linked intellectual disability 94
  • Aliases:
    • MRX94
    • MRXS29
    • mental retardation, X-linked 94
    • syndromic X-linked intellectual disability due to GRIA3 anomalies
    • syndromic X-linked mental retardation 29
    • syndromic X-linked mental retardation Wu type
Homo sapiens (human)
DOID:0080809
  • chronic asthma
Homo sapiens (human)
DOID:0050948
  • autosomal dominant hypophosphatemic rickets
Homo sapiens (human)
DOID:0050439
  • Usher syndrome
Homo sapiens (human)
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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