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 9026 - 9050 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:0070154
  • hereditary sensory neuropathy type 1F
  • Aliases:
    • HSN1F
    • hereditary sensory neuropathy type IF
Mus musculus (house mouse)
DOID:62
  • aortic valve disease
Mus musculus (house mouse)
DOID:1107
  • esophageal carcinoma
  • Aliases:
    • cancer of esophagus
    • cancer of oesophagus
    • carcinoma of esophagus
    • carcinoma of oesophagus
Mus musculus (house mouse)
DOID:0080079
  • nonsyndromic congenital nail disorder 1
  • Aliases:
    • nonsyndromic congenital nail disorder 10
    • twenty-nail dystrophy
Mus musculus (house mouse)
DOID:104
  • bacterial infectious disease
Mus musculus (house mouse)
DOID:3613
  • Canavan disease
  • Aliases:
    • ACY2 DEFICIENCY
    • AMINOACYLASE 2 DEFICIENCY
    • ASP DEFICIENCY
    • ASPA DEFICIENCY
    • ASPARTOACYLASE DEFICIENCY
    • CANAVAN-VAN BOGAERT-BERTRAND DISEASE
    • Spongy degeneration of central nervous system
Mus musculus (house mouse)
DOID:2566
  • corneal dystrophy
Mus musculus (house mouse)
DOID:0070462
  • mitochondrial complex V (ATP synthase) deficiency nuclear type 4B
  • Aliases:
    • MC5DN4B
Mus musculus (house mouse)
DOID:0090048
  • dystonia 16
Mus musculus (house mouse)
DOID:0070233
  • Loeys-Dietz syndrome 4
  • Aliases:
    • Aneurysm, aortic and cerebral, with arterial tortuosity and skeletal manifestations
    • LDS4
Mus musculus (house mouse)
DOID:0110809
  • hereditary spastic paraplegia 57
  • Aliases:
    • SPG57
    • autosomal recessive spastic paraplegia 57
    • autosomal recessive spastic paraplegia type 57
Mus musculus (house mouse)
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:0060412
  • chromosome 1q41-q42 deletion syndrome
  • Aliases:
    • 1q41-q42 microdeletion syndrome
    • 1q41q42 microdeletion syndrome
Mus musculus (house mouse)
DOID:0050637
  • Finnish type amyloidosis
  • Aliases:
    • AGel amyloidosis
    • AMYLOIDOSIS, MERETOJA TYPE
    • Lattice corneal dystrophy type II
    • gelsolin amyloidosis
Mus musculus (house mouse)
DOID:0080585
  • Van Maldergem syndrome 1
Mus musculus (house mouse)
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:0081366
  • Paget's disease of bone 3
  • Aliases:
    • Paget disease of bone-3
Mus musculus (house mouse)
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)
DOID:3587
  • pancreatic ductal carcinoma
  • Aliases:
    • malignant neoplasm of duct of Wirsung
    • pancreatic duct cancer
Mus musculus (house mouse)
DOID:0110679
  • congenital myasthenic syndrome 4C
  • Aliases:
    • CMS Id
    • CMS1D
    • CMS4C
    • FIM1
    • congenital myasthenic syndrome 4C associated with acetylcholine receptor deficiency
    • congenital myasthenic syndrome type Id
    • familial infantile myasthenia 1
Mus musculus (house mouse)
DOID:0111215
  • autosomal dominant distal hereditary motor neuronopathy 8
  • Aliases:
    • DHMN8
    • HMN8
    • autosomal dominant benign distal spinal muscular atrophy
    • autosomal dominant congenital benign spinal muscular atrophy
    • congenital benign spinal muscular atrophy with contractures
    • congenital nonprogressive spinal muscular atrophy
    • distal hereditary motor neuronopathy type 8
    • distal hereditary motor neuropathy type VIII
Mus musculus (house mouse)
DOID:0081097
  • Rafiq syndrome
  • Aliases:
    • MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
Mus musculus (house mouse)
DOID:10016
  • multiple endocrine neoplasia type 2B
  • Aliases:
    • MEN type IIB
    • MEN2B
    • Multiple endocrine neoplasia, type 3
    • Wagenmann-Froboese syndrome
    • mucosal neuroma syndrome
Mus musculus (house mouse)
DOID:10611
  • protein-losing enteropathy
  • Aliases:
    • Enteropathy, exudative
    • Exudative enteropathy
Mus musculus (house mouse)

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Last updated: December 9, 2024