GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 6476 - 6500 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:92
  • speech disorder
Homo sapiens (human)
DOID:11105
  • fundus albipunctatus
  • Aliases:
    • Pigmentary retinal dystrophy
    • retinitis punctata albescens
Homo sapiens (human)
DOID:10584
  • retinitis pigmentosa
  • Aliases:
    • pericentral pigmentary retinopathy
Homo sapiens (human)
DOID:1432
  • blindness
  • Aliases:
    • vision impairment
    • vision loss
    • visual impairment
Homo sapiens (human)
DOID:0060225
  • 3MC syndrome
  • Aliases:
    • craniofacial-ulnar-renal syndrome
    • oculopalatoskeletal syndrome
Homo sapiens (human)
DOID:0060577
  • 3MC syndrome 3
Homo sapiens (human)
DOID:0080073
  • spina bifida occulta
Homo sapiens (human)
DOID:12603
  • acute leukemia
  • Aliases:
    • Stem cell Leukemia
    • Stem cell leukaemia
Homo sapiens (human)
DOID:13994
  • cleidocranial dysplasia
  • Aliases:
    • Marie-Sainton Disease
    • cleidocranial dysostosis
Homo sapiens (human)
DOID:9827
  • radioulnar synostosis
Homo sapiens (human)
DOID:0060467
  • humeroradial synostosis
Homo sapiens (human)
DOID:1040
  • chronic lymphocytic leukemia
  • Aliases:
    • B-cell chronic lymphocytic leukaemia
    • B-cell chronic lymphocytic leukemia
    • CLL
    • chronic lymphatic leukaemia
    • chronic lymphatic leukemia
    • chronic lymphocytic leukaemia
    • lymphoplasmacytic leukaemia
    • lymphoplasmacytic leukemia
Homo sapiens (human)
DOID:1703
  • Richter's syndrome
  • Aliases:
    • Richter syndrome
Homo sapiens (human)
DOID:10426
  • Klippel-Feil syndrome
  • Aliases:
    • Klippel-Feil and Turner syndrome
    • Klippel-Feil deformity, deafness and facial asymmetry
    • autosomal dominant Klippel-Feil syndrome
    • congenital dystrophia brevicollis
    • congenital synostosis of cervical vertebrae
Homo sapiens (human)
DOID:6682
  • spondylolisthesis
Homo sapiens (human)
DOID:0060261
  • congenital ptosis
Homo sapiens (human)
DOID:0060260
  • ptosis
  • Aliases:
    • blepharoptosis
    • drooping eyelid
Homo sapiens (human)
DOID:0050908
  • myelodysplastic syndrome
Homo sapiens (human)
DOID:9296
  • cleft lip
  • Aliases:
    • Labium leporinum
    • cheiloschisis
    • cleft lip, unilateral, complete
    • complete unilateral cleft lip
    • hare lip
Homo sapiens (human)
DOID:0110213
  • isolated cleft palate
Homo sapiens (human)
DOID:674
  • cleft palate
  • Aliases:
    • Palatoschisis
Homo sapiens (human)
DOID:12858
  • Huntington's disease
  • Aliases:
    • HD
    • Huntington disease
    • Huntington's chorea
Mus musculus (house mouse)
DOID:13580
  • cholestasis
  • Aliases:
    • Obstruction of bile duct
    • bile occlusion
Mus musculus (house mouse)
DOID:219
  • colon cancer
Mus musculus (house mouse)
DOID:3908
  • lung non-small cell carcinoma
  • Aliases:
    • NSCLC
    • Non-small cell lung cancer
    • non-small cell lung carcinoma
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: August 19, 2024