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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 January 28, 2025
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 76 - 100 of 5716 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism Source
DOID:0110125
  • Bardet-Biedl syndrome 3
  • Aliases:
    • BBS3
Mus musculus (house mouse)
DOID:0110130
  • Bardet-Biedl syndrome 8
  • Aliases:
    • BBS8
Homo sapiens (human)
DOID:0110131
  • Bardet-Biedl syndrome 9
  • Aliases:
    • BBS9
Homo sapiens (human)
DOID:1935
  • Bardet-Biedl syndrome
Homo sapiens (human)
DOID:7941
  • Barrett's adenocarcinoma
  • Aliases:
    • Barrett adenocarcinoma
    • adenocarcinoma Arising in Barrett's Mucosa
Homo sapiens (human)
DOID:9206
  • Barrett's esophagus
  • Aliases:
    • Barrett esophagus
    • Barrett's esophagus with esophagitis
    • Barrett's oesophagus
    • Barrett's ulcer of esophagus
    • Barretts syndrome
    • ulcerative esophagitis
Homo sapiens (human)
DOID:9206
  • Barrett's esophagus
  • Aliases:
    • Barrett esophagus
    • Barrett's esophagus with esophagitis
    • Barrett's oesophagus
    • Barrett's ulcer of esophagus
    • Barretts syndrome
    • ulcerative esophagitis
Rattus norvegicus (Norway rat)
DOID:0050476
  • Barth syndrome
  • Aliases:
    • 3-methylglutaconicaciduria type 2
    • 3-methylglutaconicaciduria type II
    • MGA Type 2
    • MGA type II
Mus musculus (house mouse)
DOID:0110142
  • Bartter disease type 1
  • Aliases:
    • BARTS1
    • Bartter syndrome type 1
    • Bartter syndrome type 1 antenatal
    • hyperprostaglandin E syndrome 1
    • hypokalemic alkalosis with hypercalciuria 1 antenatal
Homo sapiens (human)
DOID:0110142
  • Bartter disease type 1
  • Aliases:
    • BARTS1
    • Bartter syndrome type 1
    • Bartter syndrome type 1 antenatal
    • hyperprostaglandin E syndrome 1
    • hypokalemic alkalosis with hypercalciuria 1 antenatal
Mus musculus (house mouse)
DOID:0110143
  • Bartter disease type 2
  • Aliases:
    • BARTS2
    • Bartter syndrome type 2
    • Bartter syndrome type 2 antenatal
    • hyperprostaglandin E syndrome 2
    • hypokalemic alkalosis with hypercalciuria 2 antenatal
Homo sapiens (human)
DOID:0110143
  • Bartter disease type 2
  • Aliases:
    • BARTS2
    • Bartter syndrome type 2
    • Bartter syndrome type 2 antenatal
    • hyperprostaglandin E syndrome 2
    • hypokalemic alkalosis with hypercalciuria 2 antenatal
Mus musculus (house mouse)
DOID:0110144
  • Bartter disease type 3
  • Aliases:
    • BARTS3
    • Bartter syndrome type 3
    • classic Bartter syndrome
Homo sapiens (human)
DOID:0110144
  • Bartter disease type 3
  • Aliases:
    • BARTS3
    • Bartter syndrome type 3
    • classic Bartter syndrome
Mus musculus (house mouse)
DOID:0110146
  • Bartter disease type 4b
  • Aliases:
    • BARTS4B
    • Bartter syndrome, type 4b, digenic
    • neonatal Bartter syndrome type 4B with sensorineural deafness
Homo sapiens (human)
DOID:0110147
  • Bartter disease type 5
  • Aliases:
    • BARTS5
    • Bartter syndrome, type 5, antenatal, transient
Homo sapiens (human)
DOID:445
  • Bartter disease
  • Aliases:
    • Aldosteronism with hyperplasia of the adrenal cortex
    • Bartter's syndrome
Mus musculus (house mouse)
DOID:445
  • Bartter disease
  • Aliases:
    • Aldosteronism with hyperplasia of the adrenal cortex
    • Bartter's syndrome
Homo sapiens (human)
DOID:0050660
  • Beare-Stevenson cutis gyrata syndrome
Homo sapiens (human)
DOID:0050660
  • Beare-Stevenson cutis gyrata syndrome
Mus musculus (house mouse)
DOID:9883
  • Becker muscular dystrophy
  • Aliases:
    • Benign pseudohypertrophic muscular dystrophy
    • benign congenital myopathy
Mus musculus (house mouse)
DOID:9883
  • Becker muscular dystrophy
  • Aliases:
    • Benign pseudohypertrophic muscular dystrophy
    • benign congenital myopathy
Homo sapiens (human)
DOID:5572
  • Beckwith-Wiedemann syndrome
Mus musculus (house mouse)
DOID:13241
  • Behcet's disease
  • Aliases:
    • Adamantiades-Behcet disease
    • Behcet syndrome
    • Behet's syndrome
    • triple symptom complex
Homo sapiens (human)
DOID:0111580
  • Behr syndrome
  • Aliases:
    • Abortive cerebellar ataxia (BEHRS)
    • BEHRS
    • optic atrophy in early childhood, associated with ataxia, spasticity, mental retardation, and posterior column sensory loss
    • optic atrophy, infantile hereditary, Behr complicated form of
Homo sapiens (human)
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Last updated: April 7, 2025