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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 4901 - 4925 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0110823
  • hereditary spastic paraplegia 8
  • Aliases:
    • SPG8
    • autosomal dominant spastic paraplegia 8
    • autosomal dominant spastic paraplegia type 8
Homo sapiens (human)
DOID:0110788
  • hereditary spastic paraplegia 37
  • Aliases:
    • SPG37
    • autosomal dominant spastic paraplegia 37
    • autosomal dominant spastic paraplegia type 37
Homo sapiens (human)
DOID:0110824
  • hereditary spastic paraplegia 9A
  • Aliases:
    • AD-SPG9A
    • Cataracts motor neuropathy-short stature-skeletal anomalies syndrome
    • SPG9A
    • autosomal dominant complex spastic paraplegia type 9A
    • autosomal dominant spastic paraplegia 9A
    • cataracts with motor neuronopathy, short stature and skeletal abnormalities
    • spastic paraparesis with amyopathy, cataracts and gastroesophageal reflux
    • spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome
Homo sapiens (human)
DOID:0110794
  • hereditary spastic paraplegia 42
  • Aliases:
    • SPG42
    • autosomal dominant spastic paraplegia 42
    • autosomal dominant spastic paraplegia type 42
Homo sapiens (human)
DOID:0060491
  • SPOAN syndrome
  • Aliases:
    • spastic paraplegia, optic atropy, and neuropathy
    • spastic paraplegia, optic atropy, and neuropathy syndrome
Homo sapiens (human)
DOID:0110790
  • hereditary spastic paraplegia 39
  • Aliases:
    • NTE-related motor neuron disorder
    • NTEMND
    • SPG39
    • autosomal recessive spastic paraplegia 39
    • autosomal recessive spastic paraplegia type 39
    • spastic paraplegia due to NTE mutation
    • spastic paraplegia due to neuropathy target esterase mutation
Homo sapiens (human)
DOID:0110801
  • hereditary spastic paraplegia 49
  • Aliases:
    • SPG49
    • autosomal recessive spastic paraplegia 49
    • autosomal recessive spastic paraplegia type 49
Homo sapiens (human)
DOID:0110820
  • hereditary spastic paraplegia 75
  • Aliases:
    • SPG75
    • autosomal recessive spastic paraplegia 75
    • autosomal recessive spastic paraplegia type 75
Homo sapiens (human)
DOID:0110786
  • hereditary spastic paraplegia 35
  • Aliases:
    • FAHN
    • SPG35
    • autosomal recessive spastic paraplegia 35
    • autosomal recessive spastic paraplegia type 35
    • fatty acid hydroxylase-associated neurodegeneration
    • leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia
Homo sapiens (human)
DOID:0050886
  • Troyer syndrome
  • Aliases:
    • SPG20
    • autosomal recessive spastic paraplegia 20
    • autosomal recessive spastic paraplegia Troyer type
    • autosomal recessive spastic paraplegia type 20
    • childhood-onset spastic paraparesis with distal muscle wasting
    • hereditary spastic paraplegia 20
    • spastic paraplegia 20
    • spastic paraplegia type 20
Homo sapiens (human)
DOID:2476
  • hereditary spastic paraplegia
  • Aliases:
    • French settlement disease
    • Strumpell-Lorrain disease
    • familial spastic paraplegia
    • hereditary spastic paraparesis
Homo sapiens (human)
DOID:0110816
  • hereditary spastic paraplegia 7
  • Aliases:
    • SPG7
    • autosomal recessive spastic paraplegia 7
    • spastic paraplegia type 7
Homo sapiens (human)
DOID:12680
  • pseudobulbar palsy
  • Aliases:
    • pseudobulbar paralysis
Homo sapiens (human)
DOID:0110818
  • hereditary spastic paraplegia 73
  • Aliases:
    • SPG73
    • autosomal dominant spastic paraplegia 73
    • autosomal dominant spastic paraplegia type 73
Homo sapiens (human)
DOID:0110763
  • hereditary spastic paraplegia 10
  • Aliases:
    • SPG10
    • autosomal dominant spastic paraplegia 10
    • autosomal dominant spastic paraplegia type 10
Homo sapiens (human)
DOID:4610
  • intestinal benign neoplasm
  • Aliases:
    • intestinal tumors
    • intestine growth
    • neoplasm of intestinal tract
Homo sapiens (human)
DOID:10155
  • intestinal cancer
  • Aliases:
    • malignant intestinal tumors
    • malignant neoplasm of intestine
Homo sapiens (human)
DOID:5003
  • eunuchism
Homo sapiens (human)
DOID:0060246
  • MASA syndrome
  • Aliases:
    • CRASH syndrome
    • Gareis-Mason syndrome
    • L1 syndrome
    • SPG1
    • X-linked complicated hereditary spastic paraplegia type 1
    • X-linked corpus callosum agenesis
    • X-linked spastic paraplegia 1
    • hereditary spastic paraplegia 1
Homo sapiens (human)
DOID:0080201
  • Peters plus syndrome
  • Aliases:
    • Krause-Kivlin syndrome
    • Peters anomaly-short limb dwarfism syndrome
    • Peters-plus syndrome
Rattus norvegicus (Norway rat)
DOID:0080201
  • Peters plus syndrome
  • Aliases:
    • Krause-Kivlin syndrome
    • Peters anomaly-short limb dwarfism syndrome
    • Peters-plus syndrome
Mus musculus (house mouse)
DOID:0080575
  • Larsen-like syndrome B3GAT3 type
  • Aliases:
    • Larsen-like syndrome, B3GAT3 type
    • multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome
Mus musculus (house mouse)
DOID:0080575
  • Larsen-like syndrome B3GAT3 type
  • Aliases:
    • Larsen-like syndrome, B3GAT3 type
    • multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome
Rattus norvegicus (Norway rat)
DOID:9206
  • Barrett's esophagus
  • Aliases:
    • Barrett esophagus
    • Barrett's esophagus with esophagitis
    • Barrett's oesophagus
    • Barrett's ulcer of esophagus
    • Barretts syndrome
    • ulcerative esophagitis
Rattus norvegicus (Norway rat)
DOID:9206
  • Barrett's esophagus
  • Aliases:
    • Barrett esophagus
    • Barrett's esophagus with esophagitis
    • Barrett's oesophagus
    • Barrett's ulcer of esophagus
    • Barretts syndrome
    • ulcerative esophagitis
Mus musculus (house mouse)
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Last updated: August 19, 2024