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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 October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 10976 - 11000 of 15957 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism Source
DOID:0110366
  • retinitis pigmentosa 33
  • Aliases:
    • RP33
Homo sapiens (human)
DOID:2994
  • germ cell cancer
  • Aliases:
    • malignant tumor of the germ cell
Homo sapiens (human)
DOID:0111248
  • cerebrocostomandibular syndrome
  • Aliases:
    • CCM syndrome
    • CCMS
    • cerebro-costo-mandibular syndrome
    • rib gap defects with micrognathia
Homo sapiens (human)
DOID:0110708
  • hypotrichosis 11
  • Aliases:
    • Hypt11
Homo sapiens (human)
DOID:4971
  • myelofibrosis
  • Aliases:
    • Agnogenic myeloid metaplasia
    • Aleukemic myelosis
    • Megakaryocytic myelosclerosis
    • bone Marrow Fibrosis
    • myelosclerosis
    • primary myelofibrosis
Saccharomyces cerevisiae S288C
DOID:2871
  • endometrial carcinoma
  • Aliases:
    • carcinoma of the Endometrium
    • endometrioid carcinoma
    • endometrioid carcinoma of female Reproductive system
Saccharomyces cerevisiae S288C
DOID:0080066
  • autosomal recessive spinocerebellar ataxia 20
  • Aliases:
    • SCAR20
Homo sapiens (human)
DOID:5113
  • nutritional deficiency disease
Homo sapiens (human)
DOID:3613
  • Canavan disease
  • Aliases:
    • ACY2 DEFICIENCY
    • AMINOACYLASE 2 DEFICIENCY
    • ASP DEFICIENCY
    • ASPA DEFICIENCY
    • ASPARTOACYLASE DEFICIENCY
    • CANAVAN-VAN BOGAERT-BERTRAND DISEASE
    • Spongy degeneration of central nervous system
Homo sapiens (human)
DOID:0112359
  • congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay
  • Aliases:
    • CAKUTHED
Homo sapiens (human)
DOID:0081427
  • autosomal recessive distal hereditary motor neuronopathy 8
  • Aliases:
    • SORDD
    • sorbitol dehydrogenase deficiency with peripheral neuropathy
Saccharomyces cerevisiae S288C
DOID:0081427
  • autosomal recessive distal hereditary motor neuronopathy 8
  • Aliases:
    • SORDD
    • sorbitol dehydrogenase deficiency with peripheral neuropathy
Homo sapiens (human)
DOID:0060582
  • Noonan syndrome 4
  • Aliases:
    • NS4
Homo sapiens (human)
DOID:0060466
  • gingival fibromatosis
  • Aliases:
    • hereditary gingival fibromatosis
    • hereditary gingival hyperplasia
Homo sapiens (human)
DOID:6420
  • pulmonary valve stenosis
Homo sapiens (human)
DOID:0060587
  • Noonan syndrome 9
  • Aliases:
    • NS9
Homo sapiens (human)
DOID:0080036
  • SOST-related sclerosing bone dysplasia
  • Aliases:
    • van Buchem disease
Homo sapiens (human)
DOID:0080807
  • autosomal dominant craniodiaphyseal dysplasia
Homo sapiens (human)
DOID:0060251
  • sclerosteosis
Homo sapiens (human)
DOID:0060756
  • sclerosteosis 1
  • Aliases:
    • SOST1
Homo sapiens (human)
DOID:10811
  • nasal cavity cancer
  • Aliases:
    • malignant neoplasm of nasal cavities
    • malignant tumor of the nasal cavity
Homo sapiens (human)
DOID:0111801
  • syndromic microphthalmia 3
  • Aliases:
    • AEG syndrome
    • MCOPS3
    • SOX2 anophthalmia syndrome
    • anophthalmia clinical with associated anomalies
    • anophthalmia esophageal genital syndrome
    • anophthalmia microphthalmia esophageal atresia
    • anophthalmia/microphthalmia-esophageal atresia syndrome
    • microphthalmia and esophageal atresia syndrome
    • syndromic microphthalmia type 3
Homo sapiens (human)
DOID:0050463
  • campomelic dysplasia
  • Aliases:
    • Acampomelic Campomelic Dysplasia
Homo sapiens (human)
DOID:0110348
  • osteogenesis imperfecta type 12
  • Aliases:
    • OI12
    • osteogenesis imperfecta type XII
Homo sapiens (human)
DOID:0110607
  • primary ciliary dyskinesia 28
  • Aliases:
    • CILD28
    • primary ciliary dyskinesia 28 with or without situs inversus
Homo sapiens (human)
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Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024