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 5851 - 5875 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼ Source
DOID:0080114
  • mitochondrial complex III deficiency nuclear type 5
Mus musculus (house mouse)
DOID:9446
  • cholangitis
Mus musculus (house mouse)
DOID:2044
  • drug-induced hepatitis
  • Aliases:
    • Drug-induced chronic hepatitis
Mus musculus (house mouse)
DOID:0080546
  • non-alcoholic fatty liver
  • Aliases:
    • NAFL
    • nonalcoholic fatty liver
Mus musculus (house mouse)
DOID:0060751
  • familial temporal lobe epilepsy 7
  • Aliases:
    • ETL7
Mus musculus (house mouse)
DOID:3407
  • carotid artery disease
  • Aliases:
    • disorder of carotid artery
Mus musculus (house mouse)
DOID:0060652
  • familial erythrocytosis 1
  • Aliases:
    • ECYT1
    • autosomal dominant benign erythrocytosis
    • primary familial and congenital polycythemia
Mus musculus (house mouse)
DOID:0111240
  • congenital muscular dystrophy-dystroglycanopathy type A2
  • Aliases:
    • MDDGA2
    • Walker-Warburg syndrome or muscle-eye-brain disease, POMT2-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A2
Mus musculus (house mouse)
DOID:14501
  • Sjogren-Larsson syndrome
  • Aliases:
    • FALDH deficiency
    • SLS
    • Sjogren Larsson syndrome
    • Sjogren-Larsson's syndrome
    • fatty acid alcohol oxidoreductase deficiency
Mus musculus (house mouse)
DOID:2236
  • congenital afibrinogenemia
  • Aliases:
    • Factor I deficiency
    • Fibrinogen deficiency
Mus musculus (house mouse)
DOID:0060234
  • Carpenter syndrome
  • Aliases:
    • acrocephalopolysyndactyly type II
Mus musculus (house mouse)
DOID:0112370
  • Coffin-Siris syndrome 12
  • Aliases:
    • CSS12
Mus musculus (house mouse)
DOID:11383
  • cryptorchidism
  • Aliases:
    • Cryptorchism
    • Undescended testicle
    • Undescended testis
    • undescended testicles
Mus musculus (house mouse)
DOID:0110219
  • Brugada syndrome 2
  • Aliases:
    • BRGDA2
Mus musculus (house mouse)
DOID:0080758
  • Fanconi renotubular syndrome 2
Mus musculus (house mouse)
DOID:0050457
  • Sertoli cell-only syndrome
  • Aliases:
    • DEL CASTILLO SYNDROME
    • Germinal Cell Aplasia
Mus musculus (house mouse)
DOID:0070095
  • oculocutaneous albinism type IB
  • Aliases:
    • Albinism, Yellow Mutant Type
    • OCA1B
Mus musculus (house mouse)
DOID:0040085
  • bacterial sepsis
Mus musculus (house mouse)
DOID:13628
  • favism
Mus musculus (house mouse)
DOID:0090071
  • hypogonadotropic hypogonadism 11 with or without anosmia
Mus musculus (house mouse)
DOID:0080592
  • Klippel-Feil syndrome 4
Mus musculus (house mouse)
DOID:0080155
  • very long chain acyl-CoA dehydrogenase deficiency
  • Aliases:
    • VLCAD deficiency
Mus musculus (house mouse)
DOID:0070344
  • ocular tuberculosis
Mus musculus (house mouse)
DOID:2491
  • sensory peripheral neuropathy
  • Aliases:
    • peripheral Sensory Neuropathy
    • sensory neuropathy
Mus musculus (house mouse)
DOID:0060558
  • lethal congenital contracture syndrome
Mus musculus (house mouse)

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024