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 2001 - 2025 of 4621 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Organism
DOID:0110054
  • amelogenesis imperfecta type 1A
  • Aliases:
    • AI1A
    • amelogenesis imperfecta hypoplastic type IA
    • amelogenesis imperfecta type IA
Homo sapiens (human)
DOID:0110057
  • amelogenesis imperfecta type 2A1
  • Aliases:
    • AI2A1
    • amelogenesis imperfecta pigmented hypomaturation type 1
    • amelogenesis imperfecta type IIA1
Homo sapiens (human)
DOID:0110060
  • amelogenesis imperfecta hypomaturation type 2A2
  • Aliases:
    • AI2A2
    • amelogenesis imperfecta hypomaturation type IIA2
    • amelogenesis imperfecta pigmented hypomaturation type 2
    • amelogenesis imperfecta type IIA2
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:0110053
  • amelogenesis imperfecta type 4
  • Aliases:
    • AI4
    • AIHHT
    • amelogenesis imperfecta hypomaturation-hypoplastic type with taurodontism
Homo sapiens (human)
DOID:0110059
  • X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2
  • Aliases:
    • AIH3
    • amelogenesis imperfecta type IE X-linked 2
    • amelogenesis imperfecta 3 hypoplastic type
Homo sapiens (human)
DOID:0110065
  • amelogenesis imperfecta type 1F
  • Aliases:
    • AI1F
    • amelogenesis imperfecta hypoplastic type IF
    • amelogenesis imperfecta type IF
Homo sapiens (human)
DOID:0110056
  • amelogenesis imperfecta type 1C
  • Aliases:
    • AI1C
    • amelogenesis imperfecta type IC
    • autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion
    • autosomal recessive amelogenesis imperfecta local hypoplastic type
Homo sapiens (human)
DOID:0110052
  • amelogenesis imperfecta type 1B
  • Aliases:
    • AI1B
    • AIH2
    • amelogenesis imperfecta type IB
    • autosomal dominant hypoplastic local amelogenesis imperfecta
    • hereditary localized enamel hypoplasia
Homo sapiens (human)
DOID:0110064
  • amelogenesis imperfecta type 1H
  • Aliases:
    • AI1H
    • amelogenesis imperfecta type IH
Homo sapiens (human)
DOID:4154
  • dentinogenesis imperfecta
Homo sapiens (human)
DOID:0110062
  • amelogenesis imperfecta hypomaturation type 2A4
  • Aliases:
    • AI2A4
    • amelogenesis imperfecta hypomaturation type IIA4
    • amelogenesis imperfecta type IIA4
Homo sapiens (human)
DOID:0110063
  • amelogenesis imperfecta hypomaturation type 2A5
  • Aliases:
    • AI2A5
    • amelogenesis imperfecta hypomaturation type IIA5
    • amelogenesis imperfecta type IIA5
Homo sapiens (human)
DOID:0110061
  • amelogenesis imperfecta hypomaturation type 2A3
  • Aliases:
    • AI2A3
    • amelogenesis imperfecta hypomaturation type IIA3
    • amelogenesis imperfecta type IIA3
Homo sapiens (human)
DOID:0080365
  • endometrial hyperplasia
Homo sapiens (human)
DOID:6053
  • childhood germ cell cancer
  • Aliases:
    • paediatric germ cell cancer
    • paediatric germ cell neoplasm
    • pediatric germ cell cancer
    • pediatric germ cell neoplasm
Homo sapiens (human)
DOID:4468
  • clear cell adenocarcinoma
  • Aliases:
    • Mesonephroid Clear cell carcinoma
    • Mesonephroma, malignant
    • Water-clear cell adenocarcinoma
    • Water-clear cell carcinoma
    • Wolffian duct neoplasm
    • malignant Mesonephroma
    • mesonephroma
Homo sapiens (human)
DOID:11383
  • cryptorchidism
  • Aliases:
    • Cryptorchism
    • Undescended testicle
    • Undescended testis
    • undescended testicles
Homo sapiens (human)
DOID:0090091
  • hypogonadotropic hypogonadism 23 with or without anosmia
  • Aliases:
    • 46,XY DSD due to LHB deficiency
    • 46,XY DSD due to luteinizing hormone subunit beta deficiency
    • 46,XY disorder of sex development due to LHB deficiency
    • 46,XY disorder of sex development due to luteinizing hormone subunit beta deficiency
    • Leydig cell hypoplasia due to luteinizing hormone subunit beta deficiency
    • Pasqualini syndrome
    • fertile eunuch syndrome
    • leydig cell hypoplasia due to LHB deficiency
Homo sapiens (human)
DOID:0111773
  • 46,XY sex reversal 8
  • Aliases:
    • SRXY8
    • TDD
    • male pseudohermaphroditism due to deficiency of testicular 17,20-desmolase
Homo sapiens (human)
DOID:0050639
  • primary cutaneous amyloidosis
  • Aliases:
    • PCA
    • familial primary localized cutaneous amyloidosis
Homo sapiens (human)
DOID:3907
  • lung squamous cell carcinoma
  • Aliases:
    • Epidermoid cell carcinoma of the lung
Homo sapiens (human)
DOID:345
  • uterine disease
Homo sapiens (human)
DOID:3007
  • breast ductal carcinoma
  • Aliases:
    • duct carcinoma
Homo sapiens (human)
DOID:2154
  • nephroblastoma
  • Aliases:
    • adult nephroblastoma
Homo sapiens (human)

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Last updated: August 19, 2024