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 13601 - 13625 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0060887
  • ossification of the posterior longitudinal ligament of spine
  • Aliases:
    • OPLL
Rattus norvegicus (Norway rat)
DOID:0060884
  • renal hypomagnesemia 6
  • Aliases:
    • HOMG6
Caenorhabditis elegans
DOID:0060884
  • renal hypomagnesemia 6
  • Aliases:
    • HOMG6
Homo sapiens (human)
DOID:0060884
  • renal hypomagnesemia 6
  • Aliases:
    • HOMG6
Rattus norvegicus (Norway rat)
DOID:0060884
  • renal hypomagnesemia 6
  • Aliases:
    • HOMG6
Mus musculus (house mouse)
DOID:0060884
  • renal hypomagnesemia 6
  • Aliases:
    • HOMG6
Drosophila melanogaster (fruit fly)
DOID:0060883
  • intestinal hypomagnesemia 1
  • Aliases:
    • HOMG1
    • hypomagnesemia caused by selective magnesium malabsorption
    • hypomagnesemia intestinal type 1
    • hypomagnesemic tetany
    • intestinal hypomagnesemia with secondary hypocalcemia
    • primary hypomagnesemia with secondary hypocalcemia
Homo sapiens (human)
DOID:0060882
  • renal hypomagnesemia 4
  • Aliases:
    • HOMG4
Rattus norvegicus (Norway rat)
DOID:0060882
  • renal hypomagnesemia 4
  • Aliases:
    • HOMG4
Homo sapiens (human)
DOID:0060882
  • renal hypomagnesemia 4
  • Aliases:
    • HOMG4
Mus musculus (house mouse)
DOID:0060879
  • primary hypomagnesemia
  • Aliases:
    • HOMG
    • primary familial hypomagnesemia
Homo sapiens (human)
DOID:0060879
  • primary hypomagnesemia
  • Aliases:
    • HOMG
    • primary familial hypomagnesemia
Mus musculus (house mouse)
DOID:0060879
  • primary hypomagnesemia
  • Aliases:
    • HOMG
    • primary familial hypomagnesemia
Rattus norvegicus (Norway rat)
DOID:0060878
  • hypoparathyroidism-deafness-renal disease syndrome
  • Aliases:
    • Barakat syndrome
    • HDR syndrome
    • hypoparathyroidism, sensorineural deafness, and renal disease
Homo sapiens (human)
DOID:0060877
  • bullous congenital ichthyosiform erythroderma
  • Aliases:
    • bullous type ichthyosis
    • ichthyosis bullosa of Siemens
    • superficial epidermolytic ichthyosis
Homo sapiens (human)
DOID:0060877
  • bullous congenital ichthyosiform erythroderma
  • Aliases:
    • bullous type ichthyosis
    • ichthyosis bullosa of Siemens
    • superficial epidermolytic ichthyosis
Mus musculus (house mouse)
DOID:0060875
  • isolated growth hormone deficiency type III
  • Aliases:
    • Fleisher syndrome
    • IGHD III
    • X-linked IGHD
    • X-linked agammaglobulinemia and isolated growth hormone deficiency
    • X-linked hypogammaglobulinemia and isolated growth hormone deficiency
    • X-linked isolated growth hormone deficiency
    • congenital IGHD type III
    • congenital isolated GH deficiency type III
    • congenital isolated growth hormone deficiency type III
    • growth hormone deficiency with hypogammaglobulinemia
Mus musculus (house mouse)
DOID:0060875
  • isolated growth hormone deficiency type III
  • Aliases:
    • Fleisher syndrome
    • IGHD III
    • X-linked IGHD
    • X-linked agammaglobulinemia and isolated growth hormone deficiency
    • X-linked hypogammaglobulinemia and isolated growth hormone deficiency
    • X-linked isolated growth hormone deficiency
    • congenital IGHD type III
    • congenital isolated GH deficiency type III
    • congenital isolated growth hormone deficiency type III
    • growth hormone deficiency with hypogammaglobulinemia
Homo sapiens (human)
DOID:0060874
  • isolated growth hormone deficiency type IB
  • Aliases:
    • IGHD IB
    • congenital IGHD type IB
    • congenital isolated GH deficiency type IB
    • congenital isolated growth hormone deficiency type IB
    • dwarfism of Sindh
Caenorhabditis elegans
DOID:0060874
  • isolated growth hormone deficiency type IB
  • Aliases:
    • IGHD IB
    • congenital IGHD type IB
    • congenital isolated GH deficiency type IB
    • congenital isolated growth hormone deficiency type IB
    • dwarfism of Sindh
Mus musculus (house mouse)
DOID:0060874
  • isolated growth hormone deficiency type IB
  • Aliases:
    • IGHD IB
    • congenital IGHD type IB
    • congenital isolated GH deficiency type IB
    • congenital isolated growth hormone deficiency type IB
    • dwarfism of Sindh
Homo sapiens (human)
DOID:0060874
  • isolated growth hormone deficiency type IB
  • Aliases:
    • IGHD IB
    • congenital IGHD type IB
    • congenital isolated GH deficiency type IB
    • congenital isolated growth hormone deficiency type IB
    • dwarfism of Sindh
Drosophila melanogaster (fruit fly)
DOID:0060874
  • isolated growth hormone deficiency type IB
  • Aliases:
    • IGHD IB
    • congenital IGHD type IB
    • congenital isolated GH deficiency type IB
    • congenital isolated growth hormone deficiency type IB
    • dwarfism of Sindh
Rattus norvegicus (Norway rat)
DOID:0060872
  • isolated growth hormone deficiency type II
  • Aliases:
    • IGHD II
    • autosomal dominant isolated growth hormone deficiency
    • autosomal dominant pituitary dwarfism due to isolated growth hormone deficiency
    • congenital IGHD type II
    • congenital isolated GH deficiency type II
    • congenital isolated growth hormone deficiency type II
Homo sapiens (human)
DOID:0060870
  • isolated growth hormone deficiency
  • Aliases:
    • IGHD
    • congenital IGHD
    • congenital isolated GH deficiency
    • congenital isolated growth hormone deficiency
    • familial isolated growth hormone deficiency
    • non-acquired isolated growth hormone deficiency
Caenorhabditis elegans

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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