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 2426 - 2450 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0110822
  • hereditary spastic paraplegia 77
  • Aliases:
    • SPG77
    • autosomal recessive spastic paraplegia 77
Homo sapiens (human)
DOID:0060911
  • karyomegalic interstitial nephritis
  • Aliases:
    • KIN
    • KMIN
Homo sapiens (human)
DOID:327
  • syringomyelia
Homo sapiens (human)
DOID:0080508
  • Cornelia de Lange syndrome 4
  • Aliases:
    • CDLS4
    • Cornelia De Lange syndrome 4 with or without midline brain defects
Homo sapiens (human)
DOID:0080575
  • Larsen-like syndrome B3GAT3 type
  • Aliases:
    • Larsen-like syndrome, B3GAT3 type
    • multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome
Homo sapiens (human)
DOID:0080561
  • congenital disorder of glycosylation Ii
  • Aliases:
    • congenital disorder of glycosylation 1i
Homo sapiens (human)
DOID:0111029
  • hemochromatosis type 1
  • Aliases:
    • HFE1
    • symptomatic form of HFE-related hereditary hemochromatosis
    • symptomatic form of classic hemochromatosis
    • symptomatic form of hemochromatosis type 1
Homo sapiens (human)
DOID:0110196
  • Charcot-Marie-Tooth disease type 4G
  • Aliases:
    • CMT4G
    • Charcot-Marie-Tooth neuropathy type 4G
    • HMSNR
    • autosomal recessive Charcot-Marie-Tooth disease type 4G
    • hereditary motor and sensory neuropathy Russe type
Homo sapiens (human)
DOID:0080470
  • developmental and epileptic encephalopathy 36
  • Aliases:
    • congenital disorder of glycosylation, type Is
    • early infantile epileptic encephalopathy 36
Homo sapiens (human)
DOID:0090089
  • hypogonadotropic hypogonadism 10 with or without anosmia
Homo sapiens (human)
DOID:3052
  • Balkan nephropathy
  • Aliases:
    • Balkan endemic nephropathy
    • DEFN
    • Danubian endemic familial nephropathy
Homo sapiens (human)
DOID:1849
  • cannabis dependence
Homo sapiens (human)
DOID:2942
  • bronchiolitis
Homo sapiens (human)
DOID:865
  • vasculitis
  • Aliases:
    • Angiitis
Homo sapiens (human)
DOID:3326
  • purpura
  • Aliases:
    • Purpuric disorder
Homo sapiens (human)
DOID:5052
  • melioidosis
  • Aliases:
    • Nightcliff gardener's disease
    • Pseudoglanders
    • Whitmore's disease
    • acute and fulminating melioidosis
    • subacute and chronic melioidosis
Homo sapiens (human)
DOID:0110186
  • Charcot-Marie-Tooth disease type 4D
  • Aliases:
    • CMT4D
    • Charcot-Marie-Tooth neuropathy type 4D
    • HMSN Lom type
    • HMSN-Lom
    • HMSN4D
    • HMSNL
    • autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4D
    • hereditary motor and sensory neuropathy LOM type
Homo sapiens (human)
DOID:2738
  • pseudoxanthoma elasticum
  • Aliases:
    • Gronblad-Strandberg syndrome
Homo sapiens (human)
DOID:0070195
  • X-linked chronic granulomatous disease
  • Aliases:
    • CDGX
    • X-linked chronic cytochrome b-negative granulomatous disease
Homo sapiens (human)
DOID:9820
  • central gyrate choroidal dystrophy
  • Aliases:
    • Choroidal dystrophy, serpiginous
Homo sapiens (human)
DOID:8628
  • Hodgkin's lymphoma, lymphocytic depletion
  • Aliases:
    • Hodgkin lymphoma, lymphocyte depletion
    • Hodgkin's disease, lymphocytic depletion
    • Hodgkin's lymphocytic depletion of unspecified site
    • Lymphocyte-Depleted Classical Hodgkin Lymphoma
Homo sapiens (human)
DOID:0090017
  • epidermolysis bullosa simplex with muscular dystrophy
  • Aliases:
    • epidermolysis bullosa simplex and limb-girdle muscular dystrophy
    • limb-girdle muscular dystrophy with epidermolysis bullosa simplex
Homo sapiens (human)
DOID:0110532
  • autosomal recessive nonsyndromic deafness 86
  • Aliases:
    • DFNB86
    • autosomal recessive deafness 86
Homo sapiens (human)
DOID:6126
  • anal canal carcinoma
  • Aliases:
    • anal canal and Perianal gland carcinoma
Homo sapiens (human)
DOID:0110980
  • Joubert syndrome 1
  • Aliases:
    • CORS1
    • CPD4
    • JBTS1
    • cerebellooculorenal syndrome 1
    • cerebelloparenchymal disorder IV
Homo sapiens (human)

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Last updated: August 19, 2024