GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4226 - 4250 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism Source
DOID:12716
  • newborn respiratory distress syndrome
  • Aliases:
    • HMD - Hyaline membrane disease
    • Neonatal respiratory Distress syndrome
    • hyaline membrane disease
    • pulmonary hyaline membrane disease
    • pulmonary hypoperfusion syndrome of newborn
    • respiratory distress syndrome of newborn
Danio rerio (zebrafish)
DOID:0110293
  • autosomal recessive limb-girdle muscular dystrophy type 2P
  • Aliases:
    • LGMD2P
    • MDDGC9
    • muscular dystrophy-dystroglycanopathy (limb-girdle) type C9
    • muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related
Drosophila melanogaster (fruit fly)
DOID:0110205
  • Charcot-Marie-Tooth disease dominant intermediate E
  • Aliases:
    • CMTDIE
    • Charcot-Marie-Tooth disease-nephropathy syndrome
    • Charcot-Marie-Tooth neuropathy with focal segmental glomerulonephritis
    • autosomal dominant intermediate Charcot-Marie-Tooth disease type E
Mus musculus (house mouse)
DOID:0050644
  • arterial calcification of infancy
  • Aliases:
    • generalized arterial calcification of infancy
    • idiopathic infantile arterial calcification
    • infantile arteriosclerosis
Homo sapiens (human)
DOID:4481
  • allergic rhinitis
  • Aliases:
    • Non-seasonal allergic rhinitis
    • Perenial allergic rhinitis
    • atopic rhinitis
    • hay fever
    • pollenosis
    • seasonal allergic rhinitis
Saccharomyces cerevisiae S288C
DOID:10923
  • sickle cell anemia
  • Aliases:
    • Hb SC disease
    • Hb-S/Hb-C disease
    • Hb-SS disease without crisis
    • Hemoglobin S disease without crisis
    • Sickle-cell/Hb-C disease without crisis
    • drepanocytosis
    • haemoglobin SC disease
    • hemoglobin SC disease
    • sickle cell anaemia
Drosophila melanogaster (fruit fly)
DOID:8893
  • psoriasis
Rattus norvegicus (Norway rat)
DOID:0050804
  • glioblastoma proneural subtype
Homo sapiens (human)
DOID:419
  • scleroderma
  • Aliases:
    • dermatosclerosis
Homo sapiens (human)
DOID:1686
  • glaucoma
Xenopus tropicalis (tropical clawed frog)
DOID:8456
  • choline deficiency disease
  • Aliases:
    • choline deficiency
Homo sapiens (human)
DOID:0060061
  • primary cutaneous T-cell non-Hodgkin lymphoma
  • Aliases:
    • cutaneous T cell lymphoma
    • cutaneous T-cell lymphoma
Rattus norvegicus (Norway rat)
DOID:0060412
  • chromosome 1q41-q42 deletion syndrome
  • Aliases:
    • 1q41-q42 microdeletion syndrome
    • 1q41q42 microdeletion syndrome
Mus musculus (house mouse)
DOID:0050564
  • autosomal dominant nonsyndromic deafness
  • Aliases:
    • autosomal dominant deafness
Drosophila melanogaster (fruit fly)
DOID:0050637
  • Finnish type amyloidosis
  • Aliases:
    • AGel amyloidosis
    • AMYLOIDOSIS, MERETOJA TYPE
    • Lattice corneal dystrophy type II
    • gelsolin amyloidosis
Mus musculus (house mouse)
DOID:2247
  • spondylosis
  • Aliases:
    • Lumbar spondylosis with myelopathy
    • Spondylogenic compression of lumbar spinal cord
    • Spondylogenic compression of thoracic spinal cord
    • Thoracic or lumbar spondylosis with myelopathy
    • lumbosacral spondylosis without myelopathy
    • spondylosis with myelopathy
Homo sapiens (human)
DOID:1184
  • nephrotic syndrome
Xenopus tropicalis (tropical clawed frog)
DOID:0080585
  • Van Maldergem syndrome 1
Mus musculus (house mouse)
DOID:0110515
  • autosomal recessive nonsyndromic deafness 63
  • Aliases:
    • DFNB63
    • autosomal recessive deafness 63
Homo sapiens (human)
DOID:0110066
  • amelogenesis imperfecta type 1G
  • Aliases:
    • AI1G
    • AIGFS
    • ERS
    • amelogenesis imperfecta and gingival fibromatosis syndrome
    • amelogenesis imperfecta hypoplastic with nephrocalcinosis
    • amelogenesis imperfecta type IG
    • enamel-renal syndrome
    • enamel-renal-gingival syndrome
Mus musculus (house mouse)
DOID:0080006
  • bone development disease
Rattus norvegicus (Norway rat)
DOID:0081366
  • Paget's disease of bone 3
  • Aliases:
    • Paget disease of bone-3
Mus musculus (house mouse)
DOID:0110241
  • cataract 41
  • Aliases:
    • CTRCT41
    • congenital nuclear type cataract 41
Homo sapiens (human)
DOID:14330
  • Parkinson's disease
  • Aliases:
    • Parkinson disease
    • paralysis agitans
Mus musculus (house mouse)
DOID:3347
  • osteosarcoma
  • Aliases:
    • Osteogenic sarcoma
    • Skeletal sarcoma
    • bone tissue neoplasm
    • osteoid sarcoma
Mus musculus (house mouse)

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Last updated: December 9, 2024