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 326 - 350 of 4621 in total
Disease ID Disease Name ▲ Gene Symbol Gene ID Organism
DOID:1060
  • Hartnup disease
  • Aliases:
    • Neutral 1 amino acid transport defect
    • deficiency of tryptophan oxygenase
    • neutral amino acid transport defect
Homo sapiens (human)
DOID:11123
  • Henoch-Schoenlein purpura
  • Aliases:
    • Allergic purpura
    • Autoimmune purpura
    • Henoch-Sch?nlein purpura
    • Henoch-Sch@nlein purpura
    • Henoch-Scholein purpura
    • Henoch-Schonlein Purpura
    • Purpura, autoimmune
Homo sapiens (human)
DOID:0060540
  • Hermansky-Pudlak syndrome 2
Homo sapiens (human)
DOID:0060543
  • Hermansky-Pudlak syndrome 5
Homo sapiens (human)
DOID:3753
  • Hermansky-Pudlak syndrome
Homo sapiens (human)
DOID:10487
  • Hirschsprung's disease
  • Aliases:
    • Hirschsprung disease
    • aganglionic megacolon
    • congenital megacolon
    • macrocolon
    • pelvirectal achalasia
    • total intestinal aganglionosis
Homo sapiens (human)
DOID:8651
  • Hodgkin's granuloma
  • Aliases:
    • Hodgkin granuloma
Homo sapiens (human)
DOID:8567
  • Hodgkin's lymphoma
  • Aliases:
    • HL
    • Hodgkin disease
    • Hodgkin lymphoma
    • Hodgkin's sarcoma
    • Hodgkins lymphoma
    • stage I Subdiaphragmatic Hodgkin Lymphoma
    • stage II Subdiaphragmatic Hodgkin Lymphoma
Homo sapiens (human)
DOID:8628
  • Hodgkin's lymphoma, lymphocytic depletion
  • Aliases:
    • Hodgkin lymphoma, lymphocyte depletion
    • Hodgkin's disease, lymphocytic depletion
    • Hodgkin's lymphocytic depletion of unspecified site
    • Lymphocyte-Depleted Classical Hodgkin Lymphoma
Homo sapiens (human)
DOID:8543
  • Hodgkin's lymphoma, lymphocytic-histiocytic predominance
  • Aliases:
    • Hodgkin lymphoma, lymphocyte-rich
    • Hodgkin lymphoma, lymphocytic-histiocytic predominance
    • Hodgkin's disease, lymphocyte predominance
    • Lymphocyte Rich Hodgkin's disease
Homo sapiens (human)
DOID:8654
  • Hodgkin's lymphoma, mixed cellularity
  • Aliases:
    • Hodgkin's disease, mixed cellularity
Homo sapiens (human)
DOID:8838
  • Hodgkin's lymphoma, nodular sclerosis
  • Aliases:
    • Classical Hodgkin lymphoma, nodular sclerosis
Homo sapiens (human)
DOID:0060468
  • Holt-Oram syndrome
  • Aliases:
    • atrio-digital syndrome
    • atriodigital dysplasia
    • heart-hand syndrome
Homo sapiens (human)
DOID:11486
  • Horner's syndrome
  • Aliases:
    • Bernard Horner syndrome
    • Horner syndrome
    • cervical sympathetic paralysis
Homo sapiens (human)
DOID:11166
  • Human papillomavirus infectious disease
  • Aliases:
    • HPV
Homo sapiens (human)
DOID:12858
  • Huntington's disease
  • Aliases:
    • HD
    • Huntington disease
    • Huntington's chorea
Homo sapiens (human)
DOID:0090103
  • Huntington's disease-like 1
  • Aliases:
    • HDL1
    • HLN1
    • Huntington disease-like 1
    • Huntington-like neurodegenerative disorder 1
    • autosomal dominant Huntington-like neurodegenerative disorder
    • early-onset prion disease with prominent psychiatric features
Homo sapiens (human)
DOID:0090104
  • Huntington's disease-like 2
  • Aliases:
    • HDL2
    • Huntington disease-like 2
Homo sapiens (human)
DOID:0111140
  • IGSF1 deficiency syndrome
  • Aliases:
    • CHTE
    • X-linked central congenital hypothyroidism with late-onset macroorchidism
    • X-linked central congenital hypothyroidism with late-onset testicular enlargement
    • central hypothyroidism and testicular enlargement
Homo sapiens (human)
DOID:0050885
  • IMAGe syndrome
  • Aliases:
    • intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, genital abnormalities
Homo sapiens (human)
DOID:0070029
  • ITM2B-related cerebral amyloid angiopathy 1
  • Aliases:
    • Cerebral Amyloid Angiopathy, British Type
    • FBD
    • Familial British Dementia
    • Presenile Dementia with Spastic Ataxia
Homo sapiens (human)
DOID:0070030
  • ITM2B-related cerebral amyloid angiopathy 2
  • Aliases:
    • Cerebellar Ataxia, Cataract, Deafness, and Dementia Or Psychosis
    • FDD
    • Familial Danish Dementia
    • HOOE
    • Heredopathia Ophthalmootoencephalica
Homo sapiens (human)
DOID:2986
  • IgA glomerulonephritis
  • Aliases:
    • Berger's IgA or IgG nephropathy
    • Focal Glomerulonephritis
    • IgA nephropathy
    • primary IgA nephropathy
    • segmental glomerulonephritis
Homo sapiens (human)
DOID:0080356
  • IgG4-related disease
Homo sapiens (human)
DOID:10844
  • Japanese encephalitis
  • Aliases:
    • Japanese B encephalitis
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