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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 October 9, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 13101 - 13125 of 15957 in total
Disease ID ▼ Disease Name Gene Symbol Gene ID Organism Source
DOID:0070282
  • primary autosomal recessive microcephaly 8
  • Aliases:
    • MCPH8
Homo sapiens (human)
DOID:0070281
  • primary autosomal recessive microcephaly 19
  • Aliases:
    • MCPH19
Homo sapiens (human)
DOID:0070280
  • primary autosomal recessive microcephaly 5
  • Aliases:
    • MCPH5
Homo sapiens (human)
DOID:0070279
  • primary autosomal recessive microcephaly 14
  • Aliases:
    • MCPH14
Mus musculus (house mouse)
DOID:0070279
  • primary autosomal recessive microcephaly 14
  • Aliases:
    • MCPH14
Homo sapiens (human)
DOID:0070277
  • primary autosomal recessive microcephaly 15
  • Aliases:
    • MCPH15
    • NEDMISBA
    • neurodevelopmental disorder with progressive microcephaly, spasticity, and brain imaging abnormalities
Homo sapiens (human)
DOID:0070277
  • primary autosomal recessive microcephaly 15
  • Aliases:
    • MCPH15
    • NEDMISBA
    • neurodevelopmental disorder with progressive microcephaly, spasticity, and brain imaging abnormalities
Xenopus tropicalis (tropical clawed frog)
DOID:0070277
  • primary autosomal recessive microcephaly 15
  • Aliases:
    • MCPH15
    • NEDMISBA
    • neurodevelopmental disorder with progressive microcephaly, spasticity, and brain imaging abnormalities
Mus musculus (house mouse)
DOID:0070277
  • primary autosomal recessive microcephaly 15
  • Aliases:
    • MCPH15
    • NEDMISBA
    • neurodevelopmental disorder with progressive microcephaly, spasticity, and brain imaging abnormalities
Danio rerio (zebrafish)
DOID:0070274
  • hereditary nonpolyposis colorectal cancer type 2
  • Aliases:
    • COCA2
    • FCC2
    • HNPCC2
    • familial nonpolyposis colon cancer type 2
Mus musculus (house mouse)
DOID:0070274
  • hereditary nonpolyposis colorectal cancer type 2
  • Aliases:
    • COCA2
    • FCC2
    • HNPCC2
    • familial nonpolyposis colon cancer type 2
Homo sapiens (human)
DOID:0070273
  • hereditary nonpolyposis colorectal cancer type 6
  • Aliases:
    • HNPCC6
Rattus norvegicus (Norway rat)
DOID:0070273
  • hereditary nonpolyposis colorectal cancer type 6
  • Aliases:
    • HNPCC6
Homo sapiens (human)
DOID:0070273
  • hereditary nonpolyposis colorectal cancer type 6
  • Aliases:
    • HNPCC6
Caenorhabditis elegans
DOID:0070273
  • hereditary nonpolyposis colorectal cancer type 6
  • Aliases:
    • HNPCC6
Mus musculus (house mouse)
DOID:0070272
  • hereditary nonpolyposis colorectal cancer type 5
  • Aliases:
    • HNPCC5
Mus musculus (house mouse)
DOID:0070272
  • hereditary nonpolyposis colorectal cancer type 5
  • Aliases:
    • HNPCC5
Homo sapiens (human)
DOID:0070271
  • Lynch syndrome 1
  • Aliases:
    • FCC1
    • HNPCC1
    • familial nonpolyposis colon cancer type 1
    • hereditary nonpolyposis colorectal cancer type 1
Homo sapiens (human)
DOID:0070270
  • hereditary nonpolyposis colorectal cancer type 8
  • Aliases:
    • HNPCC8
Rattus norvegicus (Norway rat)
DOID:0070270
  • hereditary nonpolyposis colorectal cancer type 8
  • Aliases:
    • HNPCC8
Homo sapiens (human)
DOID:0070270
  • hereditary nonpolyposis colorectal cancer type 8
  • Aliases:
    • HNPCC8
Mus musculus (house mouse)
DOID:0070269
  • congenital disorder of glycosylation type IIq
  • Aliases:
    • CDG IIq
    • CDG2Q
    • CDGIIdq
    • COG2-CDG
    • COG2-related congenital disorder of glycosylation
Homo sapiens (human)
DOID:0070268
  • congenital disorder of glycosylation type IIp
  • Aliases:
    • CDG IIp
    • CDG syndrome type IIp
    • CDG2P
    • CDGIIdp
    • Carbohydrate deficient glycoprotein syndrome type IIp
    • Congenital disorder of glycosylation type 2p
    • TMEM199-CDG
Homo sapiens (human)
DOID:0070267
  • congenital disorder of glycosylation type IIo
  • Aliases:
    • CCDC115-CDG
    • CDG IIo
    • CDG syndrome type IIo
    • CDG2O
    • CDGIIdo
    • Carbohydrate deficient glycoprotein syndrome type IIo
    • Congenital disorder of glycosylation type 2o
Homo sapiens (human)
DOID:0070266
  • congenital disorder of glycosylation type IIn
  • Aliases:
    • CDG IIn
    • CDG syndrome type IIn
    • CDG2N
    • CDGIIdn
    • Carbohydrate deficient glycoprotein syndrome type IIn
    • Congenital disorder of glycosylation type 2n
    • SLC39A8-CDG
Mus musculus (house mouse)
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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: December 9, 2024