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 2201 - 2225 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:4772
  • obsolete mesoblastic nephroma
Homo sapiens (human)
DOID:0110041
  • Alzheimer's disease 8
  • Aliases:
    • AD8
    • Alzheimer disease 8
    • Alzheimer disease, familial 8
    • Alzheimer's disease 8, late onset
Homo sapiens (human)
DOID:0110969
  • brachydactyly type B1
  • Aliases:
    • BDB1
Homo sapiens (human)
DOID:0111062
  • familial hypobetalipoproteinemia 1
  • Aliases:
    • FHBL1
Homo sapiens (human)
DOID:0060062
  • familial juvenile hyperuricemic nephropathy
Homo sapiens (human)
DOID:0070403
  • hypomyelinating leukodystrophy 26
  • Aliases:
    • HLD26
Homo sapiens (human)
DOID:0110439
  • dilated cardiomyopathy 1P
  • Aliases:
    • CMD1P
Homo sapiens (human)
DOID:0060239
  • Van der Woude syndrome
Homo sapiens (human)
DOID:0080036
  • SOST-related sclerosing bone dysplasia
  • Aliases:
    • van Buchem disease
Homo sapiens (human)
DOID:277
  • chorioangioma
  • Aliases:
    • Placental hemangioma
Homo sapiens (human)
DOID:0060334
  • transient neonatal diabetes mellitus
Homo sapiens (human)
DOID:0110263
  • cataract 19 multiple types
  • Aliases:
    • CTRCT19
Homo sapiens (human)
DOID:4907
  • small intestine carcinoma
  • Aliases:
    • small intestinal carcinoma
Homo sapiens (human)
DOID:0111206
  • autosomal dominant distal hereditary motor neuronopathy 2
  • Aliases:
    • HMN II
    • HMN IIA
    • HMN2
    • HMN2A
    • autosomal dominant adult spinal muscular atrophy IIA
    • distal hereditary motor neuronopathy type 2
    • distal hereditary motor neuronopathy type 2A
    • distal hereditary motor neuropathy type II
    • distal hereditary motor neuropathy type IIA
    • spinal Charcot-Marie-Tooth disease IIA
Homo sapiens (human)
DOID:0060831
  • Griscelli syndrome
  • Aliases:
    • Chediak-Higashi-like syndrome
    • Griscelli-Prunieras syndrome
    • partial albinism-immunodeficiency syndrome
Homo sapiens (human)
DOID:1388
  • Tangier disease
  • Aliases:
    • familial alpha-lipoprotein deficiency
    • familial high density lipoprotein deficiency
Homo sapiens (human)
DOID:3263
  • piebaldism
  • Aliases:
    • PIEBALD TRAIT
    • Partial albinism
Homo sapiens (human)
DOID:8505
  • dermatitis herpetiformis
  • Aliases:
    • Dermatosis herpetiformis
    • Duhring's disease
Homo sapiens (human)
DOID:0080508
  • Cornelia de Lange syndrome 4
  • Aliases:
    • CDLS4
    • Cornelia De Lange syndrome 4 with or without midline brain defects
Homo sapiens (human)
DOID:8864
  • acute monocytic leukemia
  • Aliases:
    • acute Monoblastic Leukemia and acute Monocytic Leukemia
    • acute monocytic leukaemia
    • acute monocytic leukaemia without mention of remission
    • acute monocytic leukemia without mention of remission
    • acute monocytic leukemia, FAB M5
    • acute monocytic leukemia, morphology
Homo sapiens (human)
DOID:0050753
  • cerebellar ataxia
Homo sapiens (human)
DOID:0110350
  • osteogenesis imperfecta type 6
  • Aliases:
    • OI6
    • osteogenesis imperfecta type VI
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:1470
  • major depressive disorder
  • Aliases:
    • clinical depression
    • major depression
    • recurrent major depression
    • single major depressive episode
    • unipolar depression
Homo sapiens (human)
DOID:0060283
  • peeling skin syndrome
  • Aliases:
    • deciduous skin
    • familial continuous skin peeling syndrome
    • keratosis exfoliativa congenita
    • peeling skin disease
Homo sapiens (human)

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024