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 2501 - 2525 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:8552
  • chronic myeloid leukemia
  • Aliases:
    • CML
    • CML - chronic Myelogenous Leukemia
    • Myeloid Leukemia, chronic
    • chronic granulocytic leukaemia
    • chronic granulocytic leukemia
    • chronic myelogenous leukaemia
    • chronic myelogenous leukemia
    • chronic myeloid leukaemia
Homo sapiens (human)
DOID:0112374
  • muscular dystrophy-dystroglycanopathy
  • Aliases:
    • MDDG
Homo sapiens (human)
DOID:4535
  • hypotrichosis
Homo sapiens (human)
DOID:0111044
  • gray platelet syndrome
  • Aliases:
    • BDPLT4
    • GPS
    • platelet alpha-granule deficiency
    • platelet-type bleeding disorder 4
Homo sapiens (human)
DOID:0110507
  • autosomal recessive nonsyndromic deafness 5
  • Aliases:
    • DFNB5
    • autosomal recessive deafness 5
Homo sapiens (human)
DOID:0080201
  • Peters plus syndrome
  • Aliases:
    • Krause-Kivlin syndrome
    • Peters anomaly-short limb dwarfism syndrome
    • Peters-plus syndrome
Homo sapiens (human)
DOID:0080479
  • peroxisome biogenesis disorder 4A
  • Aliases:
    • peroxisome biogenesis disorder 4A (Zellweger)
Homo sapiens (human)
DOID:9650
  • pathologic nystagmus
Homo sapiens (human)
DOID:0080067
  • Charcot-Marie-Tooth disease type 5
  • Aliases:
    • hereditary motor and sensory neuropathy with pyramidal features
Homo sapiens (human)
DOID:3612
  • retinitis
Homo sapiens (human)
DOID:3663
  • cutaneous mastocytosis
  • Aliases:
    • CM
Homo sapiens (human)
DOID:11151
  • cholecystolithiasis
Homo sapiens (human)
DOID:9835
  • refractive error
Homo sapiens (human)
DOID:206
  • hereditary multiple exostoses
  • Aliases:
    • Multiple congenital exostosis
    • Multiple exostosis syndromes
    • Osteochondromatosis syndrome
    • hereditary multiple exostoses 1
    • hereditary multiple exostoses 2
    • hereditary multiple exostoses 3
    • multiple ostechondromas
Homo sapiens (human)
DOID:0060730
  • torsion dystonia 1
  • Aliases:
    • dystonia musculorum deformans
Homo sapiens (human)
DOID:2734
  • keratosis follicularis
  • Aliases:
    • DARIER-WHITE DISEASE
    • Darier's disease
Homo sapiens (human)
DOID:0110946
  • autosomal recessive osteopetrosis 7
  • Aliases:
    • OPTB7
    • autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia
    • autosomal recessive osteopetrosis type 7
    • osteoclast-poor osteopetrosis with hypogammaglobulinemia
    • osteopetrosis-hypogammaglobulinemia syndrome
Homo sapiens (human)
DOID:12987
  • agranulocytosis
  • Aliases:
    • Granulocytopenic disorder
    • Granulopenia
    • granulocytopenia
Homo sapiens (human)
DOID:0050565
  • autosomal recessive nonsyndromic deafness
Homo sapiens (human)
DOID:11165
  • common wart
Homo sapiens (human)
DOID:0060696
  • hyperekplexia 1
  • Aliases:
    • HKPX1
Homo sapiens (human)
DOID:0060774
  • congenital diarrhea
Homo sapiens (human)
DOID:3205
  • melanotic neurilemmoma
  • Aliases:
    • Melanotic Schwannoma
    • Pigmented Neurilemmoma
    • Pigmented schwannoma
Homo sapiens (human)
DOID:474
  • histiocytoid hemangioma
  • Aliases:
    • Angiolymphoid hyperplasia with eosinophilia
    • epithelioid haemangioma
    • epithelioid hemangioma
Homo sapiens (human)
DOID:0111420
  • familial GPIHBP1 deficiency
  • Aliases:
    • familial glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 deficiency
    • hyperlipoproteinemia type 1D
    • hyperlipoproteinemia type ID
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