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 2951 - 2975 of 4621 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:0060455
  • Thiel-Behnke corneal dystrophy
  • Aliases:
    • TBCD
    • Waardenburg-Jonker corneal dystrophy
    • anterior limiting membrane dystrophy type II
    • corneal dystrophy honeycomb-shaped
    • corneal dystrophy of Bowman layer type II
Homo sapiens (human)
DOID:0050336
  • hypophosphatemia
Homo sapiens (human)
DOID:9409
  • diabetes insipidus
Homo sapiens (human)
DOID:12388
  • neurohypophyseal diabetes insipidus
  • Aliases:
    • Pituitary diabetes insipidus
    • Vasopressin deficiency
    • vasopressin defective diabetes insipidus
Homo sapiens (human)
DOID:13461
  • urethral intrinsic sphincter deficiency
  • Aliases:
    • Intrinsic (urethral) sphincter deficiency [ISD]
Homo sapiens (human)
DOID:1116
  • pertussis
  • Aliases:
    • WC - Whooping cough
    • bordetella infection
    • whooping cough
Homo sapiens (human)
DOID:999
  • hypereosinophilic syndrome
  • Aliases:
    • Eosinophilic leukocytosis
    • eosinophilia
Homo sapiens (human)
DOID:11996
  • spermatic cord torsion
  • Aliases:
    • Torsion of testicle
    • Torsion of testis
    • testicular Torsion
Homo sapiens (human)
DOID:8670
  • eating disorder
Homo sapiens (human)
DOID:724
  • female stress incontinence
  • Aliases:
    • Stress incontinence - female
    • female urinary stress incontinence
Homo sapiens (human)
DOID:12384
  • dysentery
  • Aliases:
    • Infectious diarrhea
Homo sapiens (human)
DOID:12241
  • beta thalassemia
Homo sapiens (human)
DOID:2320
  • obstructive lung disease
  • Aliases:
    • respiratory airway obstruction
Homo sapiens (human)
DOID:2214
  • obsolete inherited blood coagulation disease
Homo sapiens (human)
DOID:1247
  • blood coagulation disease
  • Aliases:
    • coagulation protein disease
    • postpartum coagulation defect
    • postpartum coagulation defect with delivery
Homo sapiens (human)
DOID:1019
  • osteomyelitis
Homo sapiens (human)
DOID:0060868
  • leukoencephalopathy with vanishing white matter
  • Aliases:
    • CACH
    • CACH/VWM
    • childhood ataxia with central nervous system hypomyelination
    • vanishing white matter leukodystrophy
Homo sapiens (human)
DOID:0050883
  • infantile cerebellar-retinal degeneration
Homo sapiens (human)
DOID:0111340
  • dominant optic atrophy plus syndrome
  • Aliases:
    • DOA+
    • optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy
Homo sapiens (human)
DOID:0111442
  • optic atrophy 9
  • Aliases:
    • OPA9
Homo sapiens (human)
DOID:0111261
  • fumarase deficiency
  • Aliases:
    • FMRD
    • fumaric aciduria
Homo sapiens (human)
DOID:0111441
  • optic atrophy 1
  • Aliases:
    • OPA1
Homo sapiens (human)
DOID:0070329
  • mitochondrial DNA depletion syndrome
  • Aliases:
    • mtDNA depletion syndrome
Homo sapiens (human)
DOID:0111218
  • Friedreich ataxia 1
  • Aliases:
    • FA1
    • FRDA1
Homo sapiens (human)
DOID:12705
  • Friedreich ataxia
  • Aliases:
    • Friedreich's ataxia
    • Friedreich's tabes
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024