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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 12851 - 12875 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:5750
  • endometrial serous adenocarcinoma
  • Aliases:
    • uterine corpus serous adenocarcinoma
    • uterine papillary serous carcinoma
    • uterine serous carcinoma
Homo sapiens (human)
DOID:4852
  • pleomorphic xanthoastrocytoma
  • Aliases:
    • Pleomorphic Xantho-astrocytoma
Homo sapiens (human)
DOID:10021
  • duodenum cancer
  • Aliases:
    • Duodenal cancer
    • cancer of duodenum
    • duodenal neoplasm
Homo sapiens (human)
DOID:3044
  • food allergy
  • Aliases:
    • food hypersensitivity
Rattus norvegicus (Norway rat)
DOID:0110847
  • xeroderma pigmentosum variant type
  • Aliases:
    • XPV
    • photosensitivity with defective DNA synthesis
    • xeroderma pigmentosum with normal DNA repair rates
Homo sapiens (human)
DOID:0050450
  • Gitelman syndrome
  • Aliases:
    • HYPOMAGNESEMIA-HYPOKALEMIA, PRIMARY RENOTUBULAR, WITH HYPOCALCIURIA
Rattus norvegicus (Norway rat)
DOID:0050770
  • polycystic liver disease
  • Aliases:
    • congenital cystic liver disease
    • congenital hepatic cyst
    • fibrocystic liver disease
Rattus norvegicus (Norway rat)
DOID:3304
  • germinoma
Rattus norvegicus (Norway rat)
DOID:0112376
  • muscular dystrophy-dystroglycanopathy type B15
  • Aliases:
    • MDDGB15
    • congenital muscular dystrophy DPM3-related
Homo sapiens (human)
DOID:0111526
  • Mullerian aplasia and hyperandrogenism
  • Aliases:
    • Mullerian duct failure and hyperandrogenism
    • WNT4 deficiency
Homo sapiens (human)
DOID:0112002
  • immunodeficiency 47
  • Aliases:
    • CDG IIs
    • CDG2S
    • CDGIIs
    • IMD47
    • congenital disorder of glycosylation type IIs
    • immunodeficiency and hepatopathy with or without neurologic features
Mus musculus (house mouse)
DOID:0081211
  • autosomal recessive intellectual developmental disorder 47
Mus musculus (house mouse)
DOID:0080771
  • beta-thalassemia major
  • Aliases:
    • Cooley's anemia
Homo sapiens (human)
DOID:14400
  • capillary leak syndrome
Homo sapiens (human)
DOID:0111133
  • focal segmental glomerulosclerosis 8
  • Aliases:
    • FSGS8
Homo sapiens (human)
DOID:0070150
  • hereditary sensory and autonomic neuropathy type 2B
  • Aliases:
    • HSAN2B
    • hereditary sensory and autonomic neuropathy type IIB
Homo sapiens (human)
DOID:0050462
  • Antley-Bixler syndrome with disordered steroidogenesis
  • Aliases:
    • trapezoidocephaly-synostosis syndrome
Homo sapiens (human)
DOID:0080925
  • cytochrome P450 oxidoreductase deficiency
Homo sapiens (human)
DOID:0081072
  • craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome
  • Aliases:
    • Cerebro-facio-thoracic dysplasia
    • Cerebrofaciothoracic dysplasia
    • Pascual-Castroviejo syndrome
    • TMCO1 defect syndrome
Homo sapiens (human)
DOID:0081124
  • craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1
Homo sapiens (human)
DOID:0050569
  • Seckel syndrome
  • Aliases:
    • Harper's syndrome
    • Virchow-Seckel dwarfism
    • bird-headed dwarfism
    • microcephalic primordial dwarfism
Homo sapiens (human)
DOID:0070007
  • Seckel syndrome 1
  • Aliases:
    • SCKL1
    • microcephalic primordial dwarfism I
Homo sapiens (human)
DOID:0111648
  • ectopia lentis with ectopia of pupil
  • Aliases:
    • ectopia lentis et pupillae
Homo sapiens (human)
DOID:0111149
  • autosomal recessive isolated ectopia lentis 2
  • Aliases:
    • ECTOL2
Homo sapiens (human)
DOID:110
  • lens disease
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