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 5226 - 5250 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:9938
  • dacryocystitis
Homo sapiens (human)
DOID:1532
  • pleural disease
  • Aliases:
    • disorder of pleura
    • non-neoplastic pleural disease
Homo sapiens (human)
DOID:9588
  • encephalitis
Homo sapiens (human)
DOID:11573
  • listeriosis
  • Aliases:
    • Infection by Listeria monocytogenes
    • Listeria infection
Homo sapiens (human)
DOID:0080297
  • Coffin-Siris syndrome 6
Drosophila melanogaster (fruit fly)
DOID:0060645
  • chronic recurrent multifocal osteomyelitis
  • Aliases:
    • CRMO
    • chronic multifocal osteomyelitis
Homo sapiens (human)
DOID:11030
  • corneal edema
  • Aliases:
    • Corneal oedema
Homo sapiens (human)
DOID:1002
  • endometritis
Homo sapiens (human)
DOID:4371
  • Schnitzler syndrome
Homo sapiens (human)
DOID:0111960
  • immunodeficiency 15A
  • Aliases:
    • IMD15A
Homo sapiens (human)
DOID:0111959
  • immunodeficiency 15B
  • Aliases:
    • IMD15B
Homo sapiens (human)
DOID:14221
  • abdominal obesity-metabolic syndrome 1
  • Aliases:
    • dysmetabolic syndrome X
    • metabolic syndrome X
Homo sapiens (human)
DOID:2475
  • chronic conjunctivitis
Homo sapiens (human)
DOID:13767
  • clonorchiasis
  • Aliases:
    • Oriental liver fluke disease
Homo sapiens (human)
DOID:6688
  • autoimmune lymphoproliferative syndrome
  • Aliases:
    • ALPS
    • Canale-Smith syndrome
Homo sapiens (human)
DOID:0050604
  • acrocapitofemoral dysplasia
Homo sapiens (human)
DOID:0111816
  • syndactyly type 1
  • Aliases:
    • SDTY1
    • chromosome 2q35 duplication syndrome
    • syndactyly, type 1, with or without craniosynostosis
Homo sapiens (human)
DOID:0110964
  • brachydactyly type A1
  • Aliases:
    • BDA1
    • Farabee type brachydactyly
Homo sapiens (human)
DOID:0080240
  • non-syndromic X-linked intellectual disability 106
  • Aliases:
    • MRX106
    • X-linked mental retardation 106
Drosophila melanogaster (fruit fly)
DOID:0111140
  • IGSF1 deficiency syndrome
  • Aliases:
    • CHTE
    • X-linked central congenital hypothyroidism with late-onset macroorchidism
    • X-linked central congenital hypothyroidism with late-onset testicular enlargement
    • central hypothyroidism and testicular enlargement
Homo sapiens (human)
DOID:0081135
  • agammaglobulinemia 2
Homo sapiens (human)
DOID:1386
  • abetalipoproteinemia
  • Aliases:
    • familial hypobetalipoproteinemia
    • microsomal triglyceride transfer protein deficiency disease
Drosophila melanogaster (fruit fly)
DOID:13810
  • familial hypercholesterolemia
  • Aliases:
    • Fredrickson type IIa hyperlipoproteinemia
    • Fredrickson type IIa lipidaemia
    • familial hyperbetalipoproteinaemia
    • familial hypercholesteremia
    • hyperbetalipoproteinemia
    • type II hyperlipidemia
Drosophila melanogaster (fruit fly)
DOID:0050585
  • congenital generalized lipodystrophy
Caenorhabditis elegans
DOID:0112300
  • spondylometaphyseal dysplasia with cone-rod dystrophy
  • Aliases:
    • SMD-CRD
    • SMDCRD
    • spondylometaphyseal dysplasia-cone-rod dystrophy syndrome
Caenorhabditis elegans

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Last updated: December 9, 2024