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 3051 - 3075 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:9368
  • keratoconjunctivitis
Homo sapiens (human)
DOID:0110448
  • dilated cardiomyopathy 1HH
  • Aliases:
    • CMD1HH
Homo sapiens (human)
DOID:11125
  • qualitative platelet defect
  • Aliases:
    • Qualitative platelet deficiency
Homo sapiens (human)
DOID:0110130
  • Bardet-Biedl syndrome 8
  • Aliases:
    • BBS8
Homo sapiens (human)
DOID:0060695
  • hyperekplexia
  • Aliases:
    • Kok disease
    • congenital stiff man syndrome
    • familial startle disease
    • hereditary hyperekplexia
    • startle disease
Homo sapiens (human)
DOID:0050884
  • triosephosphate isomerase deficiency
  • Aliases:
    • Triose phosphate-isomerase deficiency
Homo sapiens (human)
DOID:0110210
  • Charcot-Marie-Tooth disease X-linked recessive 5
  • Aliases:
    • CMT5X
    • CMTX5
    • Charcot-Marie-Tooth neuropathy X-linked recessive 5
    • Rosenberg-Chutorian syndrome
    • X-linked Charcot-Marie-Tooth disease type 5
    • optic atrophy, polyneuropathy, and deafness
Homo sapiens (human)
DOID:2582
  • acatalasia
  • Aliases:
    • acatalasemia
    • deficiency of catalase
Homo sapiens (human)
DOID:0090081
  • hypogonadotropic hypogonadism 22 with or without anosmia
Homo sapiens (human)
DOID:539
  • ophthalmoplegia
  • Aliases:
    • Total ophthalmoplegia
    • extraocular muscle paralysis
    • eye movement paralysis
    • oculomotor paralysis
Homo sapiens (human)
DOID:1984
  • rectal benign neoplasm
  • Aliases:
    • Rectal tumor
    • neoplasm of rectum
    • rectum neoplasm
Homo sapiens (human)
DOID:37
  • skin disease
  • Aliases:
    • Genodermatosis
    • skin and subcutaneous tissue disease
Homo sapiens (human)
DOID:3540
  • choroid plexus cancer
  • Aliases:
    • tumor of choroid plexus
    • tumor of the Choroid Plexus
Homo sapiens (human)
DOID:11258
  • cat-scratch disease
  • Aliases:
    • Debre's Syndrome
    • Debre-Mollaret Syndrome
    • Foshay-Mollaret Cat Scratch Fever
    • benign lymphoreticulosis
    • cat scratch fever
Homo sapiens (human)
DOID:0060182
  • microscopic colitis
Homo sapiens (human)
DOID:6496
  • obsolete extraskeletal myxoid chondrosarcoma
Homo sapiens (human)
DOID:0050861
  • colorectal adenocarcinoma
Homo sapiens (human)
DOID:5166
  • endometrial stromal tumor
  • Aliases:
    • endometrial Stromal neoplasm
Homo sapiens (human)
DOID:0110822
  • hereditary spastic paraplegia 77
  • Aliases:
    • SPG77
    • autosomal recessive spastic paraplegia 77
Homo sapiens (human)
DOID:2834
  • acquired polycythemia
  • Aliases:
    • Polycythemia, secondary
    • secondary polycythemia
Homo sapiens (human)
DOID:8368
  • chordoid meningioma
  • Aliases:
    • meningioma, chordoid
Homo sapiens (human)
DOID:0080552
  • congenital disorder of glycosylation Ia
  • Aliases:
    • PMM2-congenital disorder of glycosylation
    • congenital disorder of glycosylation 1a
Homo sapiens (human)
DOID:5296
  • liver leiomyosarcoma
  • Aliases:
    • leiomyosarcoma of the Liver
Homo sapiens (human)
DOID:0060872
  • isolated growth hormone deficiency type II
  • Aliases:
    • IGHD II
    • autosomal dominant isolated growth hormone deficiency
    • autosomal dominant pituitary dwarfism due to isolated growth hormone deficiency
    • congenital IGHD type II
    • congenital isolated GH deficiency type II
    • congenital isolated growth hormone deficiency type II
Homo sapiens (human)
DOID:0110046
  • Alzheimer's disease 13
  • Aliases:
    • AD13
    • Alzheimer disease 13
    • Alzheimer's disease 13, late onset
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024