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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 10826 - 10850 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0112164
  • spermatogenic failure 46
  • Aliases:
    • SPGF46
Homo sapiens (human)
DOID:0110599
  • primary ciliary dyskinesia 3
  • Aliases:
    • CILD3
    • primary ciliary dyskinesia 3 with or without situs inversus
Homo sapiens (human)
DOID:0112163
  • spermatogenic failure 45
  • Aliases:
    • SPGF45
Homo sapiens (human)
DOID:0111926
  • spermatogenic failure 39
  • Aliases:
    • SPGF39
Homo sapiens (human)
DOID:0110605
  • primary ciliary dyskinesia 7
  • Aliases:
    • CILD7
    • primary ciliary dyskinesia 7 with or without situs inversus
Homo sapiens (human)
DOID:0111910
  • spermatogenic failure
  • Aliases:
    • SPGF
Homo sapiens (human)
DOID:0112336
  • spermatogenic failure 56
  • Aliases:
    • SPGF56
Homo sapiens (human)
DOID:0070165
  • spermatogenic failure 18
  • Aliases:
    • SPGF18
Homo sapiens (human)
DOID:0080266
  • primary ciliary dyskinesia 37
Homo sapiens (human)
DOID:0110615
  • primary ciliary dyskinesia 25
  • Aliases:
    • CILD25
    • primary ciliary dyskinesia 25 with or without situs inversus
Homo sapiens (human)
DOID:0060254
  • Robinow syndrome
  • Aliases:
    • Robinow dwarfism
    • acral dysostosis with facial and genital abnormalities
    • fetal face syndrome
Homo sapiens (human)
DOID:4428
  • dyslexia
Homo sapiens (human)
DOID:0110626
  • primary ciliary dyskinesia 2
  • Aliases:
    • CILD2
    • primary ciliary dyskinesia 2 with or without situs inversus
Homo sapiens (human)
DOID:0110612
  • primary ciliary dyskinesia 10
  • Aliases:
    • CILD10
    • primary ciliary dyskinesia 10 with or without situs inversus
Homo sapiens (human)
DOID:0080267
  • autosomal dominant nonsyndromic deafness 71
Homo sapiens (human)
DOID:0112217
  • developmental and epileptic encephalopathy 81
  • Aliases:
    • DEE81
    • early infantile epileptic encephalopathy 81
Homo sapiens (human)
DOID:0050949
  • autosomal recessive hypophosphatemic rickets
Homo sapiens (human)
DOID:9883
  • Becker muscular dystrophy
  • Aliases:
    • Benign pseudohypertrophic muscular dystrophy
    • benign congenital myopathy
Homo sapiens (human)
DOID:0110461
  • X-linked dilated cardiomyopathy
  • Aliases:
    • CMD3B
    • DMD-related dilated cardiomyopathy
Homo sapiens (human)
DOID:0081164
  • dilated cardiomyopathy 3B
Homo sapiens (human)
DOID:264
  • hemangiopericytoma
  • Aliases:
    • Haemangiopericytic meningioma
    • hemangiopericytoma, malignant
    • malignant hemangiopericytoma
Homo sapiens (human)
DOID:799
  • varicose veins
  • Aliases:
    • Varix
    • Venous ectasia
    • Venous varices
    • varices
Homo sapiens (human)
DOID:0060072
  • benign neoplasm
Homo sapiens (human)
DOID:3650
  • lactic acidosis
Homo sapiens (human)
DOID:3649
  • pyruvate decarboxylase deficiency
  • Aliases:
    • deficiency of pyruvic dehydrogenase
    • pyruvate dehydrogenase complex deficiency disease
    • pyruvate dehydrogenase deficiency
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