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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 13451 - 13475 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Organism Source
DOID:0111797
  • autosomal recessive congenital nystagmus
  • Aliases:
    • autosomal recessive congenital motor nystagmus
Rattus norvegicus (Norway rat)
DOID:9410
  • panhypopituitarism
  • Aliases:
    • Simmond's disease
    • Simmonds' disease
    • combined pituitary hormone deficiency
Rattus norvegicus (Norway rat)
DOID:3721
  • plasmacytoma
  • Aliases:
    • Myeloma - solitary
    • Myeloma, solitary
    • Solitary myeloma
    • Solitary plasmacytoma
Rattus norvegicus (Norway rat)
DOID:9649
  • congenital nystagmus
Rattus norvegicus (Norway rat)
DOID:3877
  • functional colonic disease
Rattus norvegicus (Norway rat)
DOID:0080690
  • RASopathy
  • Aliases:
    • RAS/mitogen-activated protein kinase syndrome
Rattus norvegicus (Norway rat)
DOID:0111463
  • cardiofaciocutaneous syndrome 4
  • Aliases:
    • CFC4
Rattus norvegicus (Norway rat)
DOID:4906
  • small intestine adenocarcinoma
  • Aliases:
    • small intestinal adenocarcinoma
Rattus norvegicus (Norway rat)
DOID:0112282
  • spondyloepiphyseal dysplasia Kimberley type
  • Aliases:
    • SEDK
Rattus norvegicus (Norway rat)
DOID:2231
  • factor XII deficiency
  • Aliases:
    • Factor XII deficiency disease
    • Hageman Factor deficiency
    • deficiency, Hageman
Mus musculus (house mouse)
DOID:0080940
  • hereditary angioedema type III
Mus musculus (house mouse)
DOID:0110322
  • hypertrophic cardiomyopathy 16
  • Aliases:
    • CMH16
    • cardiomyopathy familial hypertrophic 16
Mus musculus (house mouse)
DOID:0060811
  • syndromic X-linked intellectual disability Turner type
  • Aliases:
    • Brooks-Wisniewski-Brown syndrome
    • MRXST
    • X-linked intellectual disability, Brooks type
    • mental retardation and macrocephaly syndrome
    • mental retardation, X-linked syndromic, Turner type
Mus musculus (house mouse)
DOID:0050905
  • inflammatory myofibroblastic tumor
Homo sapiens (human)
DOID:0080520
  • Tn polyagglutination syndrome
  • Aliases:
    • galactosyltransferase deficiency
Mus musculus (house mouse)
DOID:0111571
  • Weyers acrofacial dysostosis
  • Aliases:
    • Curry-Hall syndrome
    • WAD
    • Weyers acrodental dysostosis
    • acrofacial dysostosis, Weyers type
Mus musculus (house mouse)
DOID:12714
  • Ellis-Van Creveld syndrome
  • Aliases:
    • Chondroectodermal dysplasia
    • mesoectodermal dysplasia
Mus musculus (house mouse)
DOID:0081153
  • common variable immunodeficiency 11
Homo sapiens (human)
DOID:11263
  • chlamydia
  • Aliases:
    • Chlamydia trachomatis infectious disease
    • Chlamydial Infection
    • chlamydial disease
Rattus norvegicus (Norway rat)
DOID:4997
  • Camurati-Engelmann disease
  • Aliases:
    • Diaphyseal dysplasia
    • Engelman's disease
    • progressive diaphyseal dysplasia
Rattus norvegicus (Norway rat)
DOID:3227
  • tracheal stenosis
  • Aliases:
    • Stenosis of trachea
Rattus norvegicus (Norway rat)
DOID:8866
  • actinic keratosis
  • Aliases:
    • SK - Solar keratosis
    • Senile hyperkeratosis
    • Solar keratosis
    • actinic (Solar) Keratosis
Rattus norvegicus (Norway rat)
DOID:0110323
  • hypertrophic cardiomyopathy 17
  • Aliases:
    • CMH17
    • cardiomyopathy familial hypertrophic 17
Mus musculus (house mouse)
DOID:0081161
  • dilated cardiomyopathy 2E
Mus musculus (house mouse)
DOID:0060305
  • megalocornea
  • Aliases:
    • anterior megalophthalmos
    • congenital anterior megalophthalmia
Rattus norvegicus (Norway rat)
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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