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 626 - 650 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism
DOID:8574
  • lichen disease
Homo sapiens (human)
DOID:11782
  • astigmatism
Homo sapiens (human)
DOID:0080561
  • congenital disorder of glycosylation Ii
  • Aliases:
    • congenital disorder of glycosylation 1i
Mus musculus (house mouse)
DOID:11981
  • morbid obesity
  • Aliases:
    • Severe obesity
Homo sapiens (human)
DOID:8692
  • myeloid leukemia
  • Aliases:
    • Non-Lymphocytic Leukemia
    • leukaemia myelogenous
    • leukemia myelogenous
    • myeloid granulocytic leukaemia
    • myeloid granulocytic leukemia
    • myeloid leukaemia
Homo sapiens (human)
DOID:0110444
  • dilated cardiomyopathy 1X
  • Aliases:
    • CMD1X
    • dilated cardiomyopathy with mild or no proximal muscle weakness
Xenopus tropicalis (tropical clawed frog)
DOID:612
  • primary immunodeficiency disease
  • Aliases:
    • hypoimmunity
    • immune deficiency disorder
    • immunodeficiency syndrome
Rattus norvegicus (Norway rat)
DOID:5204
  • fructose-1,6-bisphosphatase deficiency
  • Aliases:
    • fructose 1 phosphate aldolase deficiency
    • fructose-1,6-diphosphatase deficiency
Rattus norvegicus (Norway rat)
DOID:0111933
  • phosphoglycerate kinase 1 deficiency
  • Aliases:
    • GSD due to phosphoglycerate kinase 1 deficiency
    • PGK1 deficiency
    • glycogen storage disease due to phosphoglycerate kinase 1 deficiency
    • glycogenosis due to phosphoglycerate kinase 1 deficiency
Drosophila melanogaster (fruit fly)
DOID:0070433
  • hyperphosphatasia with impaired intellectual development syndrome 1
  • Aliases:
    • GPIBD2
    • HPMRS1
    • glycosylphosphatidylinositol biosynthesis defect 2
    • hyperphosphatasia with mental retardation syndrome 1
Drosophila melanogaster (fruit fly)
DOID:0060337
  • CEDNIK syndrome
  • Aliases:
    • cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome
Homo sapiens (human)
DOID:0050802
  • Ehlers-Danlos syndrome spondylodysplastic type 2
  • Aliases:
    • EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 2
    • Ehlers-Danlos syndrome progeroid type
Mus musculus (house mouse)
DOID:0112298
  • spondylometaphyseal dysplasia Sedaghatian type
  • Aliases:
    • SMDS
    • Sedaghatian chondrodysplasia
    • congenital lethal metaphyseal chondrodysplasia
Saccharomyces cerevisiae S288C
DOID:0050638
  • transthyretin amyloidosis
  • Aliases:
    • ATTR amyloidosis
    • ATTRm amyloidosis
    • Amyloidosis, hereditary, transthyretin-related
    • Corino de Andrade's disease
    • Familial transthyretin amyloidosis
    • TTR amyloidosis
    • familial amyloid polyneuropathy
    • paramyloidosis
    • transthyretin-related hereditary amyloidosis
Homo sapiens (human)
DOID:11504
  • autonomic neuropathy
Homo sapiens (human)
DOID:9946
  • steroid-induced glaucoma
  • Aliases:
    • Corticosteroid-induced glaucoma
Homo sapiens (human)
DOID:8691
  • mycosis fungoides
  • Aliases:
    • mycosis fungoides lymphoma
Homo sapiens (human)
DOID:0070265
  • congenital disorder of glycosylation type IIm
  • Aliases:
    • SLC35A2-CDG
    • congenital disorder of glycosylation type 2m
    • developmental and epileptic encephalopathy 22
    • epileptic encephalopathy, early infantile, 22
Drosophila melanogaster (fruit fly)
DOID:0110238
  • cataract 18
  • Aliases:
    • CATC2
    • CTRCT18
    • autosomal recessive congenital cataract 2
    • cataract 18 autosomal recessive
Homo sapiens (human)
DOID:3326
  • purpura
  • Aliases:
    • Purpuric disorder
Homo sapiens (human)
DOID:0110435
  • dilated cardiomyopathy 1GG
  • Aliases:
    • CMD1GG
Homo sapiens (human)
DOID:0110633
  • rigid spine muscular dystrophy 1
  • Aliases:
    • Eichsfeld type congenital muscular dystrophy
    • MDRS1
    • RSMD1
    • RSS
    • SEPN1-related myopathy
    • classic MmD
    • classic multiminicore disease
    • classic multiminicore myopathy
    • congenital merosin-positive muscular dystrophy with early spine rigidity
    • desmin-related myopathy with Mallory bodies
    • desmin-related myopathy with Mallory body-like inclusions
    • early-onset desmin-related myopathy
    • rigid spine syndrome
    • severe classic form minicore myopathy
    • severe classic form multicore myopathy
    • severe classic form multiminicore disease
Homo sapiens (human)
DOID:9273
  • citrullinemia
  • Aliases:
    • ASS deficiency
    • deficiency of citrulline-aspartate ligase
Homo sapiens (human)
DOID:0111394
  • mucopolysaccharidosis type IIIB
  • Aliases:
    • MPS3B
    • MPSIIIB
    • Mucopoly-saccharidosis type 3B
    • Mucopolysaccharidosis type 3B
    • N-acetyl-alpha-glucosaminidase deficiency
    • NAGLU deficiency
    • Sanfilippo syndrome type B
    • mucopolysaccharidosis type IIIB (Sanfilippo B)
Homo sapiens (human)
DOID:2394
  • ovarian cancer
  • Aliases:
    • malignant Ovarian tumor
    • malignant tumour of ovary
    • ovarian neoplasm
    • ovary neoplasm
    • primary ovarian cancer
    • tumor of the Ovary
Drosophila melanogaster (fruit fly)

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Last updated: August 19, 2024