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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4076 - 4100 of 7942 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0060409
  • NFIA-related disorder
  • Aliases:
    • 1p31p32 microdeletion syndrome
    • Chromosome 1, Monosomy 1p32
    • brain malformations with or without urinary tract defects
    • chromosome 1p32-p31 deletion syndrome
Homo sapiens (human)
DOID:0060390
  • distal 10q deletion syndrome
  • Aliases:
    • chromosome 10q26 deletion syndrome
    • distal monosomy 10q
    • monosomy 10qter
    • telomeric deletion 10q
    • terminal chromosome 10q26 deletion syndrome
Homo sapiens (human)
DOID:1932
  • Angelman syndrome
  • Aliases:
    • happy puppet syndrome
    • puppetlike syndrome
Homo sapiens (human)
DOID:0060405
  • chromosome 17q23.1-q23.2 deletion syndrome
  • Aliases:
    • 17q23.1-q23.2 microdeletion syndrome
    • 17q23.1q23.2 microdeletion syndrome
Homo sapiens (human)
DOID:0060398
  • chromosome 16p11.2 deletion syndrome, 220-kb
  • Aliases:
    • distal 16p11.2 microdeletion syndrome
Homo sapiens (human)
DOID:0060397
  • chromosome 15q26-qter deletion syndrome
  • Aliases:
    • 15q26 deletion syndrome
    • Drayer syndrome
    • distal 15q deletion syndrome
    • distal monosomy 15q
    • telomeric 15q deletion syndrome
Homo sapiens (human)
DOID:0060404
  • chromosome 17q12 deletion syndrome
  • Aliases:
    • 17q12 microdeletion syndrome
Homo sapiens (human)
DOID:0060412
  • chromosome 1q41-q42 deletion syndrome
  • Aliases:
    • 1q41-q42 microdeletion syndrome
    • 1q41q42 microdeletion syndrome
Homo sapiens (human)
DOID:0060428
  • SATB2-associated syndrome
  • Aliases:
    • 2q32-q33 microdeletion syndrome
    • 2q32q33 microdeletion syndrome
    • Glass syndrome
    • chromosome 2q32-q33 deletion syndrome
    • monosomy 2q32
    • monosomy 2q32-q33
    • monosomy 2q32q33
Homo sapiens (human)
DOID:0060422
  • chromosome 6pter-p24 deletion syndrome
  • Aliases:
    • 6p subtelomeric deletion syndrome
    • 6p25 microdeletion syndrome
    • distal monosomy 6p
Homo sapiens (human)
DOID:0060395
  • chromosome 15q24 deletion syndrome
  • Aliases:
    • 15q24 microdeletion syndrome
Homo sapiens (human)
DOID:0060768
  • Smith-Magenis syndrome
  • Aliases:
    • 17p11.2 microdeletion syndrome
    • chromosome 17p11.2 deletion syndrome
Homo sapiens (human)
DOID:10686
  • lactocele
  • Aliases:
    • Galactocele
Homo sapiens (human)
DOID:3463
  • breast disease
Homo sapiens (human)
DOID:0070189
  • X-linked spermatogenic failure 1
  • Aliases:
    • SPGFX1
Homo sapiens (human)
DOID:10688
  • hypertrophy of breast
  • Aliases:
    • breasts enlarged
    • large breast
Homo sapiens (human)
DOID:12698
  • gynecomastia
Homo sapiens (human)
DOID:11603
  • infant gynecomastia
  • Aliases:
    • Neonatal gynaecomastia
    • breast engorgement in newborn
Homo sapiens (human)
DOID:0060076
  • estrogen-receptor negative breast cancer
Homo sapiens (human)
DOID:0070254
  • congenital disorder of glycosylation type IIb
  • Aliases:
    • CDG IIb
    • CDG2B
    • CDGIIb
    • glucosidase I deficiency
Saccharomyces cerevisiae S288C
DOID:8704
  • genital herpes
  • Aliases:
    • Genital herpes simplex
    • Herpes Genitalis
    • Virus-Genital Herpes
    • venereal herpes
Homo sapiens (human)
DOID:0080523
  • adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
  • Aliases:
    • hereditary diffuse leukoencephalopathy with spheroids
Homo sapiens (human)
DOID:0080540
  • galactosialidosis
Homo sapiens (human)
DOID:0111392
  • mucopolysaccharidosis type IVB
  • Aliases:
    • MPS IVB
    • MPS4B
    • Morquio disease type B
    • Morquio syndrome B
    • beta-D-galactosidase deficiency
    • mucopolysaccharidosis type IVB (Morquio)
Homo sapiens (human)
DOID:0111035
  • CADASIL 1
  • Aliases:
    • autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
Homo sapiens (human)
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Last updated: August 19, 2024