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 July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 1376 - 1400 of 4621 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:0060877
  • bullous congenital ichthyosiform erythroderma
  • Aliases:
    • bullous type ichthyosis
    • ichthyosis bullosa of Siemens
    • superficial epidermolytic ichthyosis
Homo sapiens (human)
DOID:2745
  • narcissistic personality disorder
Homo sapiens (human)
DOID:1509
  • avoidant personality disorder
  • Aliases:
    • anxious personality disorder
Homo sapiens (human)
DOID:0111078
  • tibial muscular dystrophy
  • Aliases:
    • Finnish tibial muscular dystrophy
    • TMD
    • Tardive tibial muscular dystrophy
    • Udd myopathy
    • Udd type distal myopathy
    • distal titinopathy
Homo sapiens (human)
DOID:0060001
  • withdrawal disorder
Homo sapiens (human)
DOID:11507
  • rumination disorder
  • Aliases:
    • Psychogenic rumination
Homo sapiens (human)
DOID:8941
  • seborrheic infantile dermatitis
  • Aliases:
    • Complement 5 dysfunction
    • Generalized seborrheic dermatitis of infants
    • Infantile seborrheic dermatitis
    • Infantile seborrhoeic dermatitis
    • Pityriasis capitis
    • Seborrhea sicca
    • Seborrhoea capitis
    • Seborrhoeic dermatitis of scalp
    • Seborrhoeic eczema of scalp
    • cradle cap
    • seborrhea capitis
Homo sapiens (human)
DOID:0060776
  • congenital diarrhea 5 with tufting enteropathy
  • Aliases:
    • DIAR5
    • congenital diarrhoea 5 with tufting enteropathy
    • congenital familial intractable diarrhea with epithelial or epithelium abnormalities
    • congenital familial intractable diarrhoea with epithelial or epithelium abnormalities
    • congenital tufting enteropathy
    • tufting enteropathy
Homo sapiens (human)
DOID:9828
  • neonatal abstinence syndrome
  • Aliases:
    • Drug withdrawal syndrome in newborn
Homo sapiens (human)
DOID:9974
  • drug dependence
Homo sapiens (human)
DOID:11382
  • corneal neovascularization
Homo sapiens (human)
DOID:0060263
  • porencephaly
Homo sapiens (human)
DOID:0112315
  • brain small vessel disease 3
  • Aliases:
    • BSVD3
Homo sapiens (human)
DOID:0060575
  • 3MC syndrome 1
Homo sapiens (human)
DOID:0060576
  • 3MC syndrome 2
Homo sapiens (human)
DOID:0060225
  • 3MC syndrome
  • Aliases:
    • craniofacial-ulnar-renal syndrome
    • oculopalatoskeletal syndrome
Homo sapiens (human)
DOID:0060577
  • 3MC syndrome 3
Homo sapiens (human)
DOID:0070298
  • multiple epiphyseal dysplasia 2
  • Aliases:
    • EDM2
Homo sapiens (human)
DOID:7489
  • Osgood-Schlatter's disease
  • Aliases:
    • Osgood-Schlatter disease
    • Osteochondritis of tibial tubercle
    • Osteochondrosis of proximal tibia
    • juvenile osteochondrosis of tibial tubercle
Homo sapiens (human)
DOID:8125
  • osteochondrosis
  • Aliases:
    • Epiphyseal necrosis
    • apophysitis
    • epiphysitis
    • osteochondritis
    • osteochondritis juvenilis
Homo sapiens (human)
DOID:0110029
  • alpha thalassemia-intellectual disability syndrome type 1
  • Aliases:
    • ATR syndrome linked to chromosome 16
    • ATR syndrome, deletion type
    • ATR-16 syndrome
    • alpha thalassemia-intellectual disability syndrome, deletion type
    • alpha thalassemia-retardation syndrome
    • alpha-thalassemia-intellectual disability syndrome linked to chromosome 16
    • alpha-thalassemia/mental retardation syndrome, deletion-type
    • alpha-thalassemia/mental retardation syndrome, type 1
Homo sapiens (human)
DOID:0110031
  • hemoglobin H disease
  • Aliases:
    • HBH
    • alpha thalassemia, haemoglobin H type
    • alpha thalassemia, hemoglobin H type
    • alpha-thalassemia intermedia
    • haemoglobin H disease
    • haemoglobin H disease, deletional
    • hemoglobin H disease, deletional
Homo sapiens (human)
DOID:0110030
  • alpha thalassemia-X-linked intellectual disability syndrome
  • Aliases:
    • ATR, nondeletion type
    • ATR-X syndrome
    • alpha-thalassemia/mental retardation syndrome nondeletion type
Homo sapiens (human)
DOID:1099
  • alpha thalassemia
  • Aliases:
    • Alpha thalassaemia
    • alpha-Thalassemia
Homo sapiens (human)
DOID:0050663
  • Bethlem myopathy
  • Aliases:
    • benign congenital muscular dystrophy
Homo sapiens (human)

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Last updated: August 19, 2024