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 4701 - 4725 of 7942 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
DOID:5348
  • adult endodermal sinus tumor
  • Aliases:
    • adult Yolk Sac neoplasm
    • adult endodermal sinus neoplasm
Homo sapiens (human)
DOID:0080844
  • omodysplasia 1
Homo sapiens (human)
DOID:0110219
  • Brugada syndrome 2
  • Aliases:
    • BRGDA2
Saccharomyces cerevisiae S288C
DOID:2951
  • motion sickness
  • Aliases:
    • Travel Sickness
Homo sapiens (human)
DOID:13580
  • cholestasis
  • Aliases:
    • Obstruction of bile duct
    • bile occlusion
Saccharomyces cerevisiae S288C
DOID:3650
  • lactic acidosis
Saccharomyces cerevisiae S288C
DOID:2754
  • glycogen storage disease VI
  • Aliases:
    • Glycogen storage disease 6
    • Hers' disease
    • glycogen storage disease type VI
    • hepatic glycogen phosphorylase deficiency
    • hepatophosphorylase deficiency glycogenosis
Saccharomyces cerevisiae S288C
DOID:2746
  • glycogen storage disease V
  • Aliases:
    • Glycogen storage disease 5
    • Glycogen storage disease, type V
    • McArdle's disease
    • glycogen storage disease type V
    • myophosphorylase deficiency
Saccharomyces cerevisiae S288C
DOID:4372
  • intracranial embolism
  • Aliases:
    • Cerebral embolism with cerebral infarction
    • cerebral embolism
Homo sapiens (human)
DOID:0050888
  • syndromic intellectual disability
Homo sapiens (human)
DOID:0060802
  • syndromic X-linked intellectual disability Snyder type
  • Aliases:
    • SRS
    • Snyder-Robinson mental retardation syndrome
    • Snyder-Robinson syndrome
    • mental retardation, X-linked, Snyder-Robinson type
    • spermine synthase deficiency
Homo sapiens (human)
DOID:0112213
  • multiple congenital anomalies-hypotonia-seizures syndrome 4
  • Aliases:
    • DEE77
    • GPIBD19
    • MCAHS4
    • developmental and epileptic encephalopathy 77
    • early infantile epileptic encephalopathy 77
    • glycosylphosphatidylinositol biosynthesis defect 19
Saccharomyces cerevisiae S288C
DOID:10112
  • sleeping sickness
  • Aliases:
    • African sleeping sickness
    • African trypanosomiasis
Saccharomyces cerevisiae S288C
DOID:0112216
  • developmental and epileptic encephalopathy 80
  • Aliases:
    • DEE80
    • GPIBD20
    • early infantile epileptic encephalopathy 80
    • glycosylphosphatidylinositol biosynthesis defect 20
Saccharomyces cerevisiae S288C
DOID:0070433
  • hyperphosphatasia with impaired intellectual development syndrome 1
  • Aliases:
    • GPIBD2
    • HPMRS1
    • glycosylphosphatidylinositol biosynthesis defect 2
    • hyperphosphatasia with mental retardation syndrome 1
Saccharomyces cerevisiae S288C
DOID:0080283
  • developmental and epileptic encephalopathy 55
  • Aliases:
    • DEE55
    • GPIBD14
    • early infantile epileptic encephalopathy 55
    • glycosylphosphatidylinositol biosynthesis defect 14
Saccharomyces cerevisiae S288C
DOID:0081223
  • glycosylphosphatidylinositol biosynthesis defect 16
  • Aliases:
    • Intellectual developmental disorder, autosomal recessive 62
Saccharomyces cerevisiae S288C
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)
DOID:0080108
  • myoglobinuria
Saccharomyces cerevisiae S288C
DOID:0111630
  • familial erythrocytosis 8
  • Aliases:
    • BPGM deficiency
    • DPGM deficiency
    • ECYT8
    • bisphosphoglycerate mutase deficiency
    • bisphosphoglyceromutase deficiency
    • diphosphoglycerate mutase deficiency of erythrocyte
    • hemolytic anemia due to diphosphoglycerate mutase deficiency
Saccharomyces cerevisiae S288C
DOID:0080932
  • primary localized cutaneous amyloidosis 3
  • Aliases:
    • Amyloidosis cutis dyschromica
Homo sapiens (human)
DOID:11758
  • iron deficiency anemia
Homo sapiens (human)
DOID:0070004
  • myeloid neoplasm
Homo sapiens (human)
DOID:9256
  • colorectal cancer
Saccharomyces cerevisiae S288C
DOID:0050861
  • colorectal adenocarcinoma
Saccharomyces cerevisiae S288C

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Last updated: August 19, 2024