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 6001 - 6025 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:0050989
  • episodic ataxia type 1
Homo sapiens (human)
DOID:4514
  • thyroid angiosarcoma
  • Aliases:
    • hemangiosarcoma of the Thyroid
Homo sapiens (human)
DOID:2474
  • vernal conjunctivitis
Homo sapiens (human)
DOID:0090100
  • ocular albinism with sensorineural deafness
  • Aliases:
    • WS2-OA
    • autosomal recessive Waardenburg syndrome type 2 with ocular albinism
    • digenic Waardenburg syndrome/albinism
    • digenic Waardenburg syndrome/ocular albinism
Homo sapiens (human)
DOID:6193
  • epithelioid sarcoma
  • Aliases:
    • epithelioid cell sarcoma
Homo sapiens (human)
DOID:3021
  • acute kidney failure
Homo sapiens (human)
DOID:6688
  • autoimmune lymphoproliferative syndrome
  • Aliases:
    • ALPS
    • Canale-Smith syndrome
Homo sapiens (human)
DOID:12144
  • low compliance bladder
  • Aliases:
    • Low bladder compliance
    • hyperactivity of bladder
    • hypertonic bladder
    • hypertonicity of bladder
Homo sapiens (human)
DOID:6741
  • bilateral breast cancer
  • Aliases:
    • Bilateral breast carcinoma
Homo sapiens (human)
DOID:3261
  • hyper IgE recurrent infection syndrome 1
  • Aliases:
    • Job syndrome
    • Job's syndrome
    • hyperimmunoglobulin E syndrome
Homo sapiens (human)
DOID:0060278
  • pontocerebellar hypoplasia type 9
Homo sapiens (human)
DOID:4254
  • osteosclerosis
Homo sapiens (human)
DOID:0070094
  • oculocutaneous albinism type IA
  • Aliases:
    • OCA1A
    • Oculocutaneous Albinism, Tyrosinase-Negative
Homo sapiens (human)
DOID:5522
  • basaloid squamous cell carcinoma
  • Aliases:
    • Basaloid carcinoma
Homo sapiens (human)
DOID:0060247
  • Smith-McCort dysplasia
Homo sapiens (human)
DOID:14400
  • capillary leak syndrome
Homo sapiens (human)
DOID:0070119
  • Meckel syndrome 5
  • Aliases:
    • MKS5
    • Meckel-Gruber syndrome, type 5
Homo sapiens (human)
DOID:12577
  • urethral obstruction
  • Aliases:
    • Obstruction of urethra
Homo sapiens (human)
DOID:0060575
  • 3MC syndrome 1
Homo sapiens (human)
DOID:0090059
  • enhanced S-cone syndrome
Homo sapiens (human)
DOID:0110452
  • dilated cardiomyopathy 1T
  • Aliases:
    • CMD1T
Homo sapiens (human)
DOID:0090087
  • hypogonadotropic hypogonadism 14 with or without anosmia
Homo sapiens (human)
DOID:4249
  • Gerstmann-Straussler-Scheinker syndrome
  • Aliases:
    • Gerstmann-Straussler-Scheinker disease
    • PRION DEMENTIA
Homo sapiens (human)
DOID:0110425
  • dilated cardiomyopathy 1A
  • Aliases:
    • CDCD1
    • dilated cardiomyopathy with conduction defect 1
    • familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Homo sapiens (human)
DOID:0050628
  • advanced sleep phase syndrome
  • Aliases:
    • familial advanced sleep-phase syndrome
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