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 July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 5526 - 5550 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:10461
  • dentin caries
  • Aliases:
    • Compound dental caries
    • Dental caries extending into dentine
Homo sapiens (human)
DOID:216
  • dental caries
  • Aliases:
    • Dental caries extending into pulp
    • Dental caries of smooth surface
    • Dental caries pit and fissure
Homo sapiens (human)
DOID:5453
  • pulmonary venoocclusive disease
  • Aliases:
    • pulmonary veno-occlusive disease
Mus musculus (house mouse)
DOID:0060350
  • adenine phosphoribosyltransferase deficiency
  • Aliases:
    • 2,8-dihydroxyadenine urolithiasis
    • APRT deficiency
Mus musculus (house mouse)
DOID:4762
  • vasculogenic impotence
Mus musculus (house mouse)
DOID:1824
  • status epilepticus
  • Aliases:
    • Grand mal status
Mus musculus (house mouse)
DOID:2106
  • myotonia congenita
  • Aliases:
    • Batten Turner congenital myopathy
    • Thomsen and Becker disease
Homo sapiens (human)
DOID:0050699
  • Dent disease
  • Aliases:
    • Dent disease 1
    • Dent disease 2
    • Dent's disease
Homo sapiens (human)
DOID:0110938
  • autosomal dominant osteopetrosis 2
  • Aliases:
    • Albers-Schonberg osteopetrosis
    • OPTA2
    • autosomal dominant Albers-Schonberg disease
    • autosomal dominant osteopetrosis type II
    • osteopetrosis autosomal dominant type 2
Homo sapiens (human)
DOID:4254
  • osteosclerosis
Homo sapiens (human)
DOID:13533
  • osteopetrosis
  • Aliases:
    • Albers-Schonberg disease
    • marble bone
Homo sapiens (human)
DOID:0110946
  • autosomal recessive osteopetrosis 7
  • Aliases:
    • OPTB7
    • autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia
    • autosomal recessive osteopetrosis type 7
    • osteoclast-poor osteopetrosis with hypogammaglobulinemia
    • osteopetrosis-hypogammaglobulinemia syndrome
Homo sapiens (human)
DOID:13922
  • eosinophilic esophagitis
Homo sapiens (human)
DOID:12336
  • male infertility
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:0112198
  • spondyloepimetaphyseal dysplasia with joint laxity type 1
  • Aliases:
    • SEMDJL1
    • spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures
Mus musculus (house mouse)
DOID:13359
  • Ehlers-Danlos syndrome
  • Aliases:
    • Cutis hyperelastica
    • elastic skin
Mus musculus (house mouse)
DOID:4450
  • renal cell carcinoma
  • Aliases:
    • RCC
    • adenocarcinoma of kidney
    • hypernephroma
Rattus norvegicus (Norway rat)
DOID:684
  • hepatocellular carcinoma
  • Aliases:
    • Hepatoma
Rattus norvegicus (Norway rat)
DOID:0050524
  • maturity-onset diabetes of the young
  • Aliases:
    • MODY
    • Mason-type diabetes
Drosophila melanogaster (fruit fly)
DOID:13317
  • hyperinsulinemic hypoglycemia
  • Aliases:
    • Islet cell hyperplasia
    • nesidioblastosis
    • persistent hyperinsulinemia hypoglycemia of infancy
Drosophila melanogaster (fruit fly)
DOID:0060639
  • permanent neonatal diabetes mellitus
  • Aliases:
    • PDMI
    • PNDM
    • permanent diabetes mellitus of infancy
Drosophila melanogaster (fruit fly)
DOID:9993
  • hypoglycemia
  • Aliases:
    • Hypoglycaemia
Drosophila melanogaster (fruit fly)
DOID:10584
  • retinitis pigmentosa
  • Aliases:
    • pericentral pigmentary retinopathy
Drosophila melanogaster (fruit fly)
DOID:0111100
  • maturity-onset diabetes of the young type 2
  • Aliases:
    • MODY glucokinase-related
    • MODY type 2
    • MODY2
Drosophila melanogaster (fruit fly)

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Last updated: August 19, 2024