GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB) and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 4801 - 4825 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:2282
  • hidradenitis
  • Aliases:
    • Hydradenitis
Homo sapiens (human)
DOID:0110031
  • hemoglobin H disease
  • Aliases:
    • HBH
    • alpha thalassemia, haemoglobin H type
    • alpha thalassemia, hemoglobin H type
    • alpha-thalassemia intermedia
    • haemoglobin H disease
    • haemoglobin H disease, deletional
    • hemoglobin H disease, deletional
Homo sapiens (human)
DOID:12594
  • Potter's syndrome
  • Aliases:
    • Potter sequence
    • Potter syndrome
Homo sapiens (human)
DOID:8503
  • impetigo herpetiformis
Homo sapiens (human)
DOID:0060536
  • mitochondrial complex I deficiency
  • Aliases:
    • isolated NADH-CoQ reductase deficiency
    • isolated NADH-coenzyme Q reductase deficiency
    • isolated NADH-ubiquinone reductase deficiency
    • isolated mitochondrial respiratory chain complex I deficiency
Homo sapiens (human)
DOID:4386
  • myofibroma
  • Aliases:
    • Lipoleiomyoma
Homo sapiens (human)
DOID:9655
  • oral mucosa leukoplakia
Homo sapiens (human)
DOID:3049
  • Churg-Strauss syndrome
  • Aliases:
    • Allergic Granulomatous Angiitis
    • Allergic granulomatosis angiitis
    • Churg-Strauss vasculitis
Homo sapiens (human)
DOID:0050817
  • Stargardt disease
  • Aliases:
    • STARGARDT DISEASE 1
Homo sapiens (human)
DOID:0110458
  • dilated cardiomyopathy 1BB
  • Aliases:
    • CMD1BB
Homo sapiens (human)
DOID:11512
  • Budd-Chiari syndrome
  • Aliases:
    • hepatic vein thrombosis
Homo sapiens (human)
DOID:0110285
  • autosomal recessive limb-girdle muscular dystrophy type 2Q
  • Aliases:
    • LGMD2Q
    • autosomal recessive limb-girdle muscular dystrophy due to plectin deficiency
    • muscular dystrophy, limb-girdle, type 2Q
Homo sapiens (human)
DOID:14464
  • neuroleptic malignant syndrome
Homo sapiens (human)
DOID:5813
  • purine nucleoside phosphorylase deficiency
  • Aliases:
    • PNP deficiency
    • Purine-Nucleoside Phosphorylase deficiency
    • deficiency of inosine phosphorylase
Homo sapiens (human)
DOID:9383
  • iridocyclitis
  • Aliases:
    • primary iridocyclitis
Homo sapiens (human)
DOID:0080210
  • primary mediastinal B-cell lymphoma
  • Aliases:
    • Large cell lymphoma of the mediastinum
    • Mediastinal diffuse large-cell lymphoma with sclerosis
    • Primary mediastinal clear cell lymphoma of B-cell type
Homo sapiens (human)
DOID:3459
  • breast carcinoma
  • Aliases:
    • Mammary carcinoma
    • carcinoma of breast
Homo sapiens (human)
DOID:1037
  • lymphoid leukemia
  • Aliases:
    • lymphoblastic leukaemia
    • lymphoblastic leukemia
    • lymphocytic leukaemia
Homo sapiens (human)
DOID:3687
  • MELAS syndrome
  • Aliases:
    • MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES
Homo sapiens (human)
DOID:10603
  • glucose intolerance
  • Aliases:
    • Glucose malabsorption
    • Malabsorption of glucose
Homo sapiens (human)
DOID:576
  • proteinuria
Homo sapiens (human)
DOID:0060854
  • autosomal recessive pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1B
    • autosomal recessive PHA 1
Homo sapiens (human)
DOID:10976
  • membranous glomerulonephritis
  • Aliases:
    • membranous nephropathy
Homo sapiens (human)
DOID:0060490
  • Schimke immuno-osseous dysplasia
  • Aliases:
    • Schimke immunoosseous dysplasia
    • Schimke syndrome
    • immunoosseous dysplasia Schimke type
    • spondyloepiphyseal dysplasia - nephrotic syndrome
Homo sapiens (human)
DOID:0112321
  • alacrima, achalasia, and impaired intellectual development syndrome
  • Aliases:
    • AAMR
    • alacrima, achalasia, and mental retardation syndrome
Homo sapiens (human)

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Last updated: August 19, 2024