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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 13776 - 13800 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0080015
  • physical disorder
  • Aliases:
    • congenital disorder
Homo sapiens (human)
DOID:668
  • myositis ossificans
  • Aliases:
    • Myisitis ossificans
    • Ossification - muscle
Homo sapiens (human)
DOID:0080313
  • cleft palate-lateral synechia syndrome
  • Aliases:
    • CPLS syndrome
    • syngnathia
Homo sapiens (human)
DOID:0080404
  • orofacial cleft 11
  • Aliases:
    • nonsyndromic cleft lip with or without cleft palate 11
Homo sapiens (human)
DOID:0080899
  • lung pleomorphic carcinoma
Homo sapiens (human)
DOID:0050641
  • Rh deficiency syndrome
Rattus norvegicus (Norway rat)
DOID:0111562
  • overhydrated hereditary stomatocytosis
  • Aliases:
    • OHS
    • potassium sodium disorder of erythrocyte
    • stomatocytosisIOHST
Rattus norvegicus (Norway rat)
DOID:0110919
  • hereditary spherocytosis type 4
  • Aliases:
    • HS4
    • SPH4
    • hereditary spherocytosis 4
Homo sapiens (human)
DOID:0110832
  • Usher syndrome type 1F
  • Aliases:
    • USH1F
    • Usher syndrome type IF
Homo sapiens (human)
DOID:0110481
  • autosomal recessive nonsyndromic deafness 23
  • Aliases:
    • DFNB23
    • autosomal recessive deafness 23
Homo sapiens (human)
DOID:0060565
  • Ritscher-Schinzel syndrome
  • Aliases:
    • CCC dysplasia
    • craniocerebellocardiac dysplasia
Mus musculus (house mouse)
DOID:0111498
  • combined oxidative phosphorylation deficiency 22
  • Aliases:
    • COXPD22
Rattus norvegicus (Norway rat)
DOID:0070462
  • mitochondrial complex V (ATP synthase) deficiency nuclear type 4B
  • Aliases:
    • MC5DN4B
Rattus norvegicus (Norway rat)
DOID:0070461
  • mitochondrial complex V (ATP synthase) deficiency nuclear type 4A
  • Aliases:
    • MC5DN4A
Rattus norvegicus (Norway rat)
DOID:0060805
  • Prieto syndrome
  • Aliases:
    • Prieto-Badia-Mulas syndrome
    • X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome
Homo sapiens (human)
DOID:4751
  • striatonigral degeneration
Rattus norvegicus (Norway rat)
DOID:0112185
  • thyroid dyshormonogenesis 1
  • Aliases:
    • TDH1
    • genetic defect in thyroid hormonogenesis 1
    • iodide accumulation, transport, or trapping defect
Homo sapiens (human)
DOID:0060306
  • Meier-Gorlin syndrome
  • Aliases:
    • ear-patella-short stature syndrome
Homo sapiens (human)
DOID:0070489
  • classic dopamine transporter deficiency syndrome
  • Aliases:
    • PKDYS1
    • classic DTDS
    • infantile parkinsonism-dystonia 1
Homo sapiens (human)
DOID:11569
  • neurocirculatory asthenia
  • Aliases:
    • Cardiovascular malfunction arising from mental factors
    • Cardiovascular neurosis
    • Da Costa's syndrome
    • Krishaber's disease
Homo sapiens (human)
DOID:0060131
  • alexithymia
Homo sapiens (human)
DOID:7475
  • diverticulitis
Homo sapiens (human)
DOID:0050800
  • cerebral creatine deficiency syndrome 1
  • Aliases:
    • CEREBRAL CREATINE DEFICIENCY SYNDROME 1
    • SLC6A8 deficiency
    • creatine transporter deficiency
Homo sapiens (human)
DOID:0110982
  • Joubert syndrome 13
  • Aliases:
    • JBTS13
Mus musculus (house mouse)
DOID:0080065
  • autosomal recessive spinocerebellar ataxia 19
  • Aliases:
    • Lichtenstein-Knorr syndrome
    • SCAR19
Homo sapiens (human)
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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