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 1551 - 1575 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Organism
DOID:0090015
  • Cenani-Lenz syndactyly syndrome
  • Aliases:
    • syndactyly type 7
Homo sapiens (human)
DOID:5656
  • cranial nerve disease
  • Aliases:
    • Cranial nerve disorder
    • disorder of cranial nerve
Homo sapiens (human)
DOID:3817
  • cranial nerve palsy
  • Aliases:
    • Cranial nerve Paralysis
Homo sapiens (human)
DOID:4624
  • Ollier disease
  • Aliases:
    • DYSCHONDROPLASIA
    • ENCHONDROMATOSIS, MULTIPLE
    • Enchondromatosis with haemangiomata
    • Kast's syndrome
    • OSTEOCHONDROMATOSIS
Homo sapiens (human)
DOID:0112263
  • hypoinsulinemic hypoglycemia with hemihypertrophy
  • Aliases:
    • HIHGHH
    • hypoinsulinemic hypoglycemia and body hemihypertrophy
Homo sapiens (human)
DOID:0081002
  • Cowden syndrome 6
Homo sapiens (human)
DOID:13482
  • Proteus syndrome
  • Aliases:
    • Wiedemann's syndrome
Homo sapiens (human)
DOID:1245
  • vulva cancer
  • Aliases:
    • Ca vulva
    • Vulvar tumor
    • malignant Vulvar tumor
    • malignant neoplasm of vulva
    • malignant tumor of vulva
    • neoplasm of vulva
    • vulval cancer
    • vulval neoplasm
    • vulvar neoplasm
Homo sapiens (human)
DOID:11342
  • arcus senilis
  • Aliases:
    • Arcus of cornea
    • corneal arcus
Homo sapiens (human)
DOID:0050475
  • Weill-Marchesani syndrome
  • Aliases:
    • GEMSS syndrome
    • Marchesani-Weill Syndrome
    • Mesodermal Dysmorphodystrophy, Congenital
    • Spherophakia Brachymorphia Syndrome
    • congenital mesodermal dystrophy
Homo sapiens (human)
DOID:0060715
  • autosomal recessive congenital ichthyosis 6
  • Aliases:
    • ARCI6
Homo sapiens (human)
DOID:0060719
  • autosomal recessive congenital ichthyosis 10
  • Aliases:
    • ARCI10
Homo sapiens (human)
DOID:0060711
  • autosomal recessive congenital ichthyosis 3
  • Aliases:
    • ARCI3
    • lamellar ichthyosis 5
Homo sapiens (human)
DOID:0060716
  • autosomal recessive congenital ichthyosis 7
  • Aliases:
    • ARCI7
Homo sapiens (human)
DOID:0060717
  • autosomal recessive congenital ichthyosis 8
  • Aliases:
    • ARCI8
    • lamellar ichthyosis 4
    • late-onset lamellar ichthyosis
Homo sapiens (human)
DOID:0060712
  • autosomal recessive congenital ichthyosis 4A
  • Aliases:
    • ARCI4A
    • ICR2B
    • ichthyosis congenita IIB
    • lamellar ichthyosis 2
Homo sapiens (human)
DOID:0060710
  • autosomal recessive congenital ichthyosis 2
  • Aliases:
    • ARCI2
    • BROCQ congenital ichthyosiform erythroderma nonbullous form
    • NCIE1
    • nonbullous congenital ichthyosiform erythroderma 1
Homo sapiens (human)
DOID:0060718
  • autosomal recessive congenital ichthyosis 9
  • Aliases:
    • ARCI9
Homo sapiens (human)
DOID:0050428
  • nonepidermolytic palmoplantar keratoderma
  • Aliases:
    • Thost-Unna Syndrome
    • Unna-Thost Syndrome
    • diffuse nonepidermolytic palmomplantar keratoderma
    • tylosis
Homo sapiens (human)
DOID:3390
  • palmoplantar keratosis
  • Aliases:
    • Keratosis palmaris et plantaris
    • Palmoplantar Keratoderma
    • palmo-plantar keratodermas
Homo sapiens (human)
DOID:2685
  • ossifying fibromyxoid tumor
  • Aliases:
    • Ossifying Fibromyxoma
    • ossifying fibromyxoid tumour
Homo sapiens (human)
DOID:2768
  • transient tic disorder
Homo sapiens (human)
DOID:2769
  • tic disorder
Homo sapiens (human)
DOID:10600
  • chronic tic disorder
  • Aliases:
    • chronic motor or vocal tic disorder
Homo sapiens (human)
DOID:10175
  • optic papillitis
  • Aliases:
    • papillitis
Homo sapiens (human)

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Last updated: August 19, 2024