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 1676 - 1700 of 4621 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▼
DOID:1019
  • osteomyelitis
Homo sapiens (human)
DOID:13938
  • amenorrhea
  • Aliases:
    • absence of menstruation
    • amenia
Homo sapiens (human)
DOID:0110527
  • autosomal recessive nonsyndromic deafness 8
  • Aliases:
    • DFNB10
    • DFNB8
    • NRSD8
    • autosomal recessive deafness 10
    • autosomal recessive deafness 8
    • childhood-onset neurosensory autosomal recessive deafness 8
    • neurosensory nonsyndromic recessive deafness 8
Homo sapiens (human)
DOID:0090117
  • thiamine-responsive megaloblastic anemia syndrome
  • Aliases:
    • Rogers syndrome
    • THMD1
    • TRMA
    • thiamine metabolism dysfunction syndrome 1
    • thiamine-responsive anaemia syndrome
    • thiamine-responsive anemia syndrome
    • thiamine-responsive megaloblastic anaemia syndrome
    • thiamine-responsive megaloblastic anaemia with diabetes mellitus and sensorineural deafness
    • thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural deafness
    • thiamine-responsive myelodysplasia
Homo sapiens (human)
DOID:8881
  • rosacea
  • Aliases:
    • Acne roscea
    • Acne, erythematosa
Homo sapiens (human)
DOID:13252
  • mesenteric vascular occlusion
Homo sapiens (human)
DOID:0090111
  • PCWH syndrome
  • Aliases:
    • Neurologic Waardenburg-Shah syndrome
    • PCWH
    • Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease
    • Peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Hirschsprung disease-Waardenburg syndrome
Homo sapiens (human)
DOID:0110270
  • cataract 17 multiple types
  • Aliases:
    • CTRCT17
Homo sapiens (human)
DOID:6658
  • pulmonary large cell neuroendocrine carcinoma
Homo sapiens (human)
DOID:3361
  • childhood osteosarcoma
  • Aliases:
    • pediatric osteosarcoma
Homo sapiens (human)
DOID:11721
  • glycogen storage disease VII
  • Aliases:
    • Glycogen storage disease 7
    • Glycogen storage disease, type VII
    • Muscle phosphofructokinase deficiency
    • glycogen storage disease type VII
    • phosphofructokinase myopathy
Homo sapiens (human)
DOID:9778
  • irritable bowel syndrome
  • Aliases:
    • IBD
    • Irritable colon
Homo sapiens (human)
DOID:0080390
  • nephrotic syndrome type 1
  • Aliases:
    • Finnish congenital nephrosis
Homo sapiens (human)
DOID:0060277
  • pontocerebellar hypoplasia type 8
Homo sapiens (human)
DOID:0050167
  • autoimmune polyendocrine syndrome type 1
  • Aliases:
    • Autoimmune Polyglandular Syndrome I
    • Whitaker syndrome
    • autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy
Homo sapiens (human)
DOID:1789
  • benign peritoneal mesothelioma
  • Aliases:
    • Mesothelioma of Peritoneum
Homo sapiens (human)
DOID:0090083
  • hypogonadotropic hypogonadism 2 with or without anosmia
Homo sapiens (human)
DOID:0060258
  • reticulate acropigmentation of Kitamura
  • Aliases:
    • RAPK
Homo sapiens (human)
DOID:0110055
  • amelogenesis imperfecta type 3A
  • Aliases:
    • ADHCAI
    • amelogenesis imperfecta hypomineralization type
    • amelogenesis imperfecta type III
    • autosomal dominant amelogenesis imperfecta hypocalcification type
Homo sapiens (human)
DOID:0070328
  • adult hepatocellular carcinoma
  • Aliases:
    • adult hepatoma
    • adult primary hepatocellular carcinoma
Homo sapiens (human)
DOID:607
  • paraplegia
  • Aliases:
    • Paraplegia, lower
Homo sapiens (human)
DOID:0050657
  • Bannayan-Riley-Ruvalcaba syndrome
  • Aliases:
    • Bannayan-Zonana syndrome
    • Cowden syndrome 1
    • Riley-Smith syndrome
    • Ruvalcaba-Myhre-Smith syndrome
Homo sapiens (human)
DOID:14447
  • gonadal dysgenesis
  • Aliases:
    • Gonadal dysgenesis syndrome
Homo sapiens (human)
DOID:6676
  • Froelich syndrome
  • Aliases:
    • Babinski-Froelich syndrome
    • Froehlich syndrome
    • Froehlich's syndrome
    • Froelich's syndrome
    • adiposogenital syndrome
Homo sapiens (human)
DOID:5003
  • eunuchism
Homo sapiens (human)

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Last updated: August 19, 2024