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 2151 - 2175 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:8233
  • inflammatory liposarcoma
Homo sapiens (human)
DOID:162
  • cancer
  • Aliases:
    • malignant neoplasm
    • malignant tumor
    • primary cancer
Homo sapiens (human)
DOID:13328
  • diabetic cataract
  • Aliases:
    • Cataract - diabetic
Homo sapiens (human)
DOID:3652
  • Leigh disease
  • Aliases:
    • Infantile necrotizing encephalomyelopathy
    • Leigh syndrome
    • juvenile subacute necrotizing encephalomyelopathy
Homo sapiens (human)
DOID:0110211
  • Charcot-Marie-Tooth disease X-linked recessive 3
  • Aliases:
    • CMT3X
    • CMTX3
    • Charcot-Marie-Tooth neuropathy X-linked recessive 3
    • X-linked Charcot-Marie-Tooth disease type 3
Homo sapiens (human)
DOID:971
  • tendinitis
Homo sapiens (human)
DOID:9563
  • bronchiectasis
  • Aliases:
    • Polynesian bronchiectasis
Homo sapiens (human)
DOID:5563
  • malignant teratoma
  • Aliases:
    • Immature teratoma
    • Teratoma, malignant, NOS
    • malignant Extragonadal teratoma
    • primary malignant extragonadal teratoma
Homo sapiens (human)
DOID:5602
  • T-cell adult acute lymphocytic leukemia
  • Aliases:
    • ATLL
    • Acute Adult T-cell Leukemia-Lymphoma
    • adult Precursor T Lymphoblastic Leukemia
Homo sapiens (human)
DOID:0050697
  • chorioamnionitis
Homo sapiens (human)
DOID:0110590
  • autosomal dominant nonsyndromic deafness 69
  • Aliases:
    • DCUA
    • DFNA69
    • autosomal dominant deafness 69
    • unilateral or asymmetric congenital deafness
Homo sapiens (human)
DOID:0110797
  • hereditary spastic paraplegia 45
  • Aliases:
    • SPG45
    • SPG65
    • autosomal recessive spastic paraplegia 45
    • autosomal recessive spastic paraplegia type 45
    • autosomal recessive spastic paraplegia type 65
Homo sapiens (human)
DOID:0080240
  • non-syndromic X-linked intellectual disability 106
  • Aliases:
    • MRX106
    • X-linked mental retardation 106
Homo sapiens (human)
DOID:14118
  • familial lipoprotein lipase deficiency
  • Aliases:
    • Fredrickson type I hyperlipoproteinemia
    • Fredrickson type I lipaemia
    • familial LPL deficiency
    • familial hyperlipoproteinemia type I
    • hypercholesterinaemic xanthomatosis
    • hyperchylomicronemia
    • mixed hyperglyceridemia
Homo sapiens (human)
DOID:2834
  • acquired polycythemia
  • Aliases:
    • Polycythemia, secondary
    • secondary polycythemia
Homo sapiens (human)
DOID:0110698
  • hypotrichosis 1
  • Aliases:
    • Hhs
    • Hts
    • Hypt1
    • hereditary generalized hypotrichosis simplex
Homo sapiens (human)
DOID:0090086
  • hypogonadotropic hypogonadism 6 with or without anosmia
Homo sapiens (human)
DOID:0080473
  • developmental delay and seizures with or without movement abnormalities
Homo sapiens (human)
DOID:0111062
  • familial hypobetalipoproteinemia 1
  • Aliases:
    • FHBL1
Homo sapiens (human)
DOID:100
  • intestinal infectious disease
  • Aliases:
    • bacterial enteritis
Homo sapiens (human)
DOID:0110439
  • dilated cardiomyopathy 1P
  • Aliases:
    • CMD1P
Homo sapiens (human)
DOID:0050848
  • obstructive sleep apnea
  • Aliases:
    • obstructive sleep apnea syndrome
Homo sapiens (human)
DOID:1926
  • Gaucher's disease
  • Aliases:
    • Gaucher disease
    • acid beta-glucosidase deficiency
    • glocucerebrosidase deficiency
    • glucosylceramide beta-glucosidase deficiency
    • kerasin thesaurismosis
Homo sapiens (human)
DOID:8536
  • herpes zoster
  • Aliases:
    • Shingles
    • herpes zona
Homo sapiens (human)
DOID:150
  • disease of mental health
Homo sapiens (human)

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Last updated: August 19, 2024