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 5476 - 5500 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:7327
  • pseudosarcomatous fibromatosis
  • Aliases:
    • Fasciitis - nodular
    • Pseudosarcomatous Fasciitis
    • nodular fasciitis
Homo sapiens (human)
DOID:0111646
  • congenital lactase deficiency
  • Aliases:
    • CLD
    • congenital alactasia
    • congenital alactasia syndrome
    • congenital lactose intolerance
    • congenital lactose malabsorption
    • disaccharide intolerance II
Homo sapiens (human)
DOID:0111385
  • inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1
  • Aliases:
    • IBMPFD1
    • MSP1
    • multisystem proteinopathy 1
Homo sapiens (human)
DOID:438
  • autoimmune disease of the nervous system
Homo sapiens (human)
DOID:0111680
  • essential fructosuria
  • Aliases:
    • fructokinase deficiency
    • hepatic fructokinase deficiency
    • ketohexokinase deficiency
Homo sapiens (human)
DOID:0111425
  • restrictive cardiomyopathy 1
  • Aliases:
    • RCM1
    • familial restrictive cardiomyopathy 1
Homo sapiens (human)
DOID:0060592
  • B-cell adult acute lymphocytic leukemia
  • Aliases:
    • B-cell adult acute lymphocytic leukaemia
    • adult B acute lymphoblastic leukaemia
    • adult B acute lymphoblastic leukemia
    • adult B-lymphoblastic leukaemia
    • adult B-lymphoblastic leukemia
    • adult b-cell acute lymphoblastic leukaemia
    • adult b-cell acute lymphoblastic leukemia
    • adult b-cell lymphocytic leukaemia
    • adult b-cell lymphocytic leukemia
Homo sapiens (human)
DOID:0110294
  • autosomal recessive limb-girdle muscular dystrophy type 2T
  • Aliases:
    • LGMD2T
    • MDDGC14
    • muscular dystrophy limb-girdle type 2T
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C14
    • muscular dystrophy-dystroglycanopathy limb-girdle GMPPB-related
Homo sapiens (human)
DOID:0111387
  • familial isolated hypoparathyroidism
  • Aliases:
    • FIH
Homo sapiens (human)
DOID:4271
  • microsporidiosis
  • Aliases:
    • Infection by Microspora
    • Infection by Microsporea
    • Infection by Microsporida
Homo sapiens (human)
DOID:0050801
  • androgenic alopecia
  • Aliases:
    • alopecia androgenetica, male pattern baldness
    • androgenetic alopecia
Homo sapiens (human)
DOID:8826
  • colon carcinoma in situ
  • Aliases:
    • carcinoma in situ of colon
    • stage 0 Colonic carcinoma
Homo sapiens (human)
DOID:5246
  • obsolete hilar cholangiocellular carcinoma
Homo sapiens (human)
DOID:0111005
  • cone-rod dystrophy 2
  • Aliases:
    • CORD2
    • CRD2
    • RCRD2
    • cone-rod retinal dystrophy 2
    • retinal cone-rod dystrophy 2
Homo sapiens (human)
DOID:3302
  • chordoma
  • Aliases:
    • notochordoma
Homo sapiens (human)
DOID:1936
  • atherosclerosis
Homo sapiens (human)
DOID:11212
  • hydrophthalmos
Homo sapiens (human)
DOID:0080582
  • hypotrichosis 14
Homo sapiens (human)
DOID:3083
  • chronic obstructive pulmonary disease
  • Aliases:
    • COLD
    • COPD
    • chronic obstructive airway disease
    • chronic obstructive lung disease
Homo sapiens (human)
DOID:0060712
  • autosomal recessive congenital ichthyosis 4A
  • Aliases:
    • ARCI4A
    • ICR2B
    • ichthyosis congenita IIB
    • lamellar ichthyosis 2
Homo sapiens (human)
DOID:2920
  • membranoproliferative glomerulonephritis
  • Aliases:
    • Lobular glomerulonephritis
    • chronic glomerulonephritis, lobular
Homo sapiens (human)
DOID:3500
  • gallbladder adenocarcinoma
  • Aliases:
    • adenocarcinoma of the gallbladder
Homo sapiens (human)
DOID:1068
  • juvenile glaucoma
  • Aliases:
    • Glaucoma of childhood
Homo sapiens (human)
DOID:3883
  • Lynch syndrome
  • Aliases:
    • COCA 1
    • HNPCC - hereditary nonpolyposis colon cancer
    • Hereditary Defective Mismatch Repair syndrome
    • Hereditary non-polyposis colon cancer
    • Hereditary non-polyposis colon cancer syndrome
    • Hereditary non-polyposis colorectal cancer
    • Hereditary non-polyposis colorectal cancer syndrome
    • Hereditary nonpolyposis colon cancer
    • Hereditary nonpolyposis colon cancer syndrome
    • Hereditary nonpolyposis colorectal cancer syndrome
    • hereditary nonpolyposis colorectal cancer
    • hereditary nonpolyposis colorectal neoplasm
Homo sapiens (human)
DOID:0110751
  • type 1 diabetes mellitus 12
  • Aliases:
    • IDDM12
    • Insulin-Dependent Diabetes Mellitus 12
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