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 376 - 400 of 4621 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism
DOID:0060294
  • cold-induced sweating syndrome
  • Aliases:
    • Crisponi syndrome
    • Sohar-Crisponi syndrome
Homo sapiens (human)
DOID:0060295
  • complement component 2 deficiency
Homo sapiens (human)
DOID:0060297
  • complement component 4a deficiency
Homo sapiens (human)
DOID:0060298
  • complement component 4b deficiency
Homo sapiens (human)
DOID:0060299
  • complement component 6 deficiency
Homo sapiens (human)
DOID:0060300
  • complement component 7 deficiency
Homo sapiens (human)
DOID:0060301
  • type I complement component 8 deficiency
Homo sapiens (human)
DOID:0060302
  • type II complement component 8 deficiency
Homo sapiens (human)
DOID:0060303
  • complement component 9 deficiency
Homo sapiens (human)
DOID:0060305
  • megalocornea
  • Aliases:
    • anterior megalophthalmos
    • congenital anterior megalophthalmia
Homo sapiens (human)
DOID:0060306
  • Meier-Gorlin syndrome
  • Aliases:
    • ear-patella-short stature syndrome
Homo sapiens (human)
DOID:0060307
  • autosomal dominant intellectual developmental disorder
  • Aliases:
    • autosomal dominant mental retardation
    • autosomal dominant non-syndromic mental retardation
Homo sapiens (human)
DOID:0060308
  • autosomal recessive intellectual developmental disorder
  • Aliases:
    • autosomal recessive mental retardation
    • autosomal recessive non-syndromic mental retardation
Homo sapiens (human)
DOID:0060309
  • syndromic X-linked intellectual disability
  • Aliases:
    • syndromic X-linked mental retardation
Homo sapiens (human)
DOID:0060311
  • adenoid hypertrophy
  • Aliases:
    • adenoidal hypertrophy
    • enlarged adenoids
Homo sapiens (human)
DOID:0060312
  • angular cheilitis
  • Aliases:
    • angular cheilosis
    • angular stomatitis
    • cheilosis
    • commissural cheilitis
Homo sapiens (human)
DOID:0060316
  • orofaciodigital syndrome I
  • Aliases:
    • Papillon-Leage-Psaume syndrome
    • orofaciodigital syndrome 1
    • orofaciodigital syndrome type I
Homo sapiens (human)
DOID:0060317
  • lung abscess
Homo sapiens (human)
DOID:0060318
  • acute promyelocytic leukemia
  • Aliases:
    • acute myeloblastic leukaemia type 3
    • acute myeloblastic leukemia type 3
    • acute myeloid leukaemia M3
    • acute myeloid leukemia M3
    • acute promyelocytic leukaemia
Homo sapiens (human)
DOID:0060319
  • cardiac arrest
  • Aliases:
    • cardiopulmonary arrest
    • circulatory arrest
Homo sapiens (human)
DOID:0060320
  • inguinal hernia
Homo sapiens (human)
DOID:0060321
  • umbilical hernia
Homo sapiens (human)
DOID:0060322
  • mastoiditis
Homo sapiens (human)
DOID:0060326
  • myelomeningocele
Homo sapiens (human)
DOID:0060327
  • omphalocele
  • Aliases:
    • omphalocoele
Homo sapiens (human)

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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