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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 6801 - 6825 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:0110703
  • hypotrichosis 6
  • Aliases:
    • Hypotrichosis, Localized, Autosomal Recessive 1
    • Hypt6
    • Lah1
    • Monilethrix-like hypotrichosis
    • autosomal recessive localized hypotrichosis
Rattus norvegicus (Norway rat)
DOID:0080038
  • pycnodysostosis
Rattus norvegicus (Norway rat)
DOID:0080195
  • Marinesco-Sjogren syndrome
  • Aliases:
    • Garland-Moorhouse syndrome
    • Marinesco-Garland syndrome
    • Oligophrenic cerebellolenticular degeneration
    • hereditary oligophrenic cerebello-lental degeneration
Rattus norvegicus (Norway rat)
DOID:9277
  • primary cerebellar degeneration
Rattus norvegicus (Norway rat)
DOID:0060486
  • Perry syndrome
  • Aliases:
    • parkinsonism with alveolar hypoventilation and mental depression
Rattus norvegicus (Norway rat)
DOID:0111202
  • autosomal dominant distal hereditary motor neuronopathy 14
  • Aliases:
    • DHMN7B
    • HMN VIIB
    • HMN7B
    • Harper-Young myopathy
    • distal hereditary motor neuronopathy type 7B
    • distal hereditary motor neuropathy type VIIB
    • distal spinal muscular atrophy with vocal cord paralysis type 7B
Rattus norvegicus (Norway rat)
DOID:0050890
  • synucleinopathy
  • Aliases:
    • Synucleinopathies
    • alpha Synucleinopathies
Rattus norvegicus (Norway rat)
DOID:0110865
  • congenital stationary night blindness 1B
  • Aliases:
    • CSNB1B
    • autosomal recessive complete congenital stationary night blindness
    • congenital stationary night blindness 1B autosomal recessive
Homo sapiens (human)
DOID:0070136
  • autosomal dominant cutis laxa 2
  • Aliases:
    • ADCL2
Rattus norvegicus (Norway rat)
DOID:0070135
  • autosomal recessive cutis laxa type IA
  • Aliases:
    • ARCL1A
Rattus norvegicus (Norway rat)
DOID:0070231
  • benign recurrent intrahepatic cholestasis 1
  • Aliases:
    • BRIC type 1
    • BRIC1
    • Summerskill syndrome
Rattus norvegicus (Norway rat)
DOID:0070228
  • intrahepatic cholestasis of pregnancy 1
  • Aliases:
    • ICP1
    • pregnancy related cholestasis 1
Rattus norvegicus (Norway rat)
DOID:0070226
  • progressive familial intrahepatic cholestasis 1
  • Aliases:
    • FIC1 deficiency
    • PFIC1
Rattus norvegicus (Norway rat)
DOID:0111072
  • myostatin-related muscle hypertrophy
  • Aliases:
    • MSLHP
Rattus norvegicus (Norway rat)
DOID:0070418
  • vertebral hypersegmentation and orofacial anomalies
  • Aliases:
    • VHO
Rattus norvegicus (Norway rat)
DOID:9245
  • Alagille syndrome
  • Aliases:
    • Alagille-Watson syndrome
    • Arteriohepatic dysplasia
Rattus norvegicus (Norway rat)
DOID:0060672
  • Grn-related frontotemporal lobar degeneration with Tdp43 inclusions
Rattus norvegicus (Norway rat)
DOID:0110732
  • neuronal ceroid lipofuscinosis 11
  • Aliases:
    • CLN11
Rattus norvegicus (Norway rat)
DOID:0060445
  • congenital stromal corneal dystrophy
  • Aliases:
    • CSCD
    • congenital hereditary stromal dystrophy
Rattus norvegicus (Norway rat)
DOID:13359
  • Ehlers-Danlos syndrome
  • Aliases:
    • Cutis hyperelastica
    • elastic skin
Rattus norvegicus (Norway rat)
DOID:8469
  • influenza
  • Aliases:
    • Influenza with other manifestations
    • flu
    • influenza with non-respiratory manifestation
Homo sapiens (human)
DOID:0080159
  • Cryptococcal meningitis
Homo sapiens (human)
DOID:0050523
  • adult T-cell leukemia/lymphoma
  • Aliases:
    • Adult T-cell leukemia/lymphoma (HTLV-1 positive)
    • adult T-cell leukemia
Homo sapiens (human)
DOID:14780
  • KBG syndrome
Homo sapiens (human)
DOID:0111230
  • congenital muscular dystrophy-dystroglycanopathy type A11
  • Aliases:
    • MDDGA11
    • Walker-Warburg syndrome or muscle-eye-brain disease B3GALNT2-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A11
Rattus norvegicus (Norway rat)
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Last updated: December 9, 2024