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 14501 - 14525 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism Source
DOID:0080600
  • COVID-19
  • Aliases:
    • 2019 Novel Coronavirus (2019-nCoV)
    • 2019-nCoV infection
    • COVID19
    • SARS-CoV-2 infection
    • Wuhan coronavirus infection
    • Wuhan seafood market pneumonia virus infection
Mus musculus (house mouse)
DOID:10591
  • pre-eclampsia
  • Aliases:
    • gestational hypertension
    • hypertension induced by pregnancy
    • pre-eclamptic toxaemia
    • preeclampsia
    • preeclampsia/eclampsia
    • pregnancy associated hypertension
    • pregnancy toxemia
    • proteinuric hypertension of pregnancy
    • toxaemia of pregnancy
Mus musculus (house mouse)
DOID:13241
  • Behcet's disease
  • Aliases:
    • Adamantiades-Behcet disease
    • Behcet syndrome
    • Behet's syndrome
    • triple symptom complex
Mus musculus (house mouse)
DOID:8947
  • diabetic retinopathy
  • Aliases:
    • Retinal abnormality - diabetes-related
Mus musculus (house mouse)
DOID:1967
  • leiomyosarcoma
  • Aliases:
    • Leiomyosarcomas
Mus musculus (house mouse)
DOID:4441
  • dysgerminoma
Mus musculus (house mouse)
DOID:0050791
  • persistent Mullerian duct syndrome
  • Aliases:
    • persistent Muellerian duct syndrome
Mus musculus (house mouse)
DOID:0080909
  • castration-resistant prostate carcinoma
Homo sapiens (human)
DOID:0111238
  • congenital muscular dystrophy-dystroglycanopathy type A13
  • Aliases:
    • MDDGA13
    • Walker-Warburg syndrome or muscle-eye-brain disease, B3GNT1-related
    • Walker-Warburg syndrome or muscle-eye-brain disease, B4GNT1-related
    • congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A13
Homo sapiens (human)
DOID:0060302
  • type II complement component 8 deficiency
Mus musculus (house mouse)
DOID:1312
  • focal segmental glomerulosclerosis
  • Aliases:
    • FGS
    • FSGS
    • focal glomerular sclerosis
    • focal glomerulosclerosis
Mus musculus (house mouse)
DOID:0110087
  • asphyxiating thoracic dystrophy 3
  • Aliases:
    • ATD3
    • SRPS1
    • SRPS2B
    • SRPS3
    • SRTD3
    • Saldino-Noonan syndrome
    • Verma-Naumoff syndrome
    • polydactyly with neonatal chondrodystrophy, type I
    • polydactyly with neonatal chondrodystrophy, type III
    • short rib-polydactyly syndrome, type I
    • short rib-polydactyly syndrome, type IIB
    • short-rib thoracic dysplasia 3 with or without polydactyly
Mus musculus (house mouse)
DOID:0050592
  • asphyxiating thoracic dystrophy
  • Aliases:
    • Jeune syndrome
    • short-rib thoracic dysplasia with or without polydactyly
    • thoracic pelvic phalangeal dystrophy
Mus musculus (house mouse)
DOID:0050563
  • nonsyndromic deafness
  • Aliases:
    • nonsyndromic hearing loss
    • nonsyndromic hereditary hearing loss
Mus musculus (house mouse)
DOID:0080547
  • metabolic dysfunction-associated steatohepatitis
  • Aliases:
    • MASH
    • NASH
    • non-alcoholic steatohepatitis
    • nonalcoholic steatohepatitis
Homo sapiens (human)
DOID:0070494
  • mitochondrial complex IV deficiency nuclear type 7
  • Aliases:
    • MC4DN7
Mus musculus (house mouse)
DOID:890
  • mitochondrial encephalomyopathy
Mus musculus (house mouse)
DOID:3587
  • pancreatic ductal carcinoma
  • Aliases:
    • malignant neoplasm of duct of Wirsung
    • pancreatic duct cancer
Mus musculus (house mouse)
DOID:0111346
  • epidermolysis bullosa simplex with mottled pigmentation
  • Aliases:
    • EBSMP
    • Epidermolysis bullosa simplex-MP
    • speckled hyperpigmentation with punctate palmoplantar keratoses and childhood blistering
Mus musculus (house mouse)
DOID:0060735
  • epidermolysis bullosa simplex Dowling-Meara type
  • Aliases:
    • EBS-gen sev
    • EBSDM
    • epidermolysis bullosa herpetiformis Dowling-Meara type
    • epidermolysis bullosa simplex, herpetiformis
    • generalized severe epidermolysis bullosa simplex
Mus musculus (house mouse)
DOID:0060256
  • Dowling-Degos disease
  • Aliases:
    • dark dot disease
    • reticular pigment anomaly of flexures
Mus musculus (house mouse)
DOID:4644
  • epidermolysis bullosa simplex
Mus musculus (house mouse)
DOID:11054
  • urinary bladder cancer
  • Aliases:
    • bladder cancer
    • tumor of the bladder
Mus musculus (house mouse)
DOID:0110671
  • congenital myasthenic syndrome 6
  • Aliases:
    • CMS Ia2
    • CMS1A2
    • CMS6
    • CMSEA
    • FIM
    • FIMG2
    • congenital myasthenic syndrome 6, presynaptic
    • congenital myasthenic syndrome type Ia2
    • congenital presynaptic myasthenic syndrome associated with episodic apnea
    • familial infantile myasthenia
    • familial infantile myasthenia gravis 2
Homo sapiens (human)
DOID:3635
  • congenital myasthenic syndrome
Homo sapiens (human)

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Last updated: December 9, 2024