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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 6676 - 6700 of 15957 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism Source
DOID:0090085
  • hypogonadotropic hypogonadism 9 with or without anosmia
Homo sapiens (human)
DOID:0111822
  • CHILD syndrome
  • Aliases:
    • CHILD nevus
    • congenital hemidysplasia with ichthyosiform nevus and limbs defects
Homo sapiens (human)
DOID:0111898
  • CK syndrome
  • Aliases:
    • X-linked intellectual disability-microcephaly-cortical malformation-thin habitus syndrome
Homo sapiens (human)
DOID:12305
  • Bloch-Sulzberger syndrome
  • Aliases:
    • Incontinentia pigmenti
    • Incontinentia pigmenti syndrome
Homo sapiens (human)
DOID:14748
  • Sotos syndrome
  • Aliases:
    • cerebral gigantism
Homo sapiens (human)
DOID:0112103
  • Sotos syndrome 1
  • Aliases:
    • SOTOS1
Homo sapiens (human)
DOID:0111332
  • Pitt-Hopkins-like syndrome 2
  • Aliases:
    • PTHSL2
Homo sapiens (human)
DOID:0070082
  • schizophrenia 6
  • Aliases:
    • SCZD6
Homo sapiens (human)
DOID:0060584
  • Noonan syndrome 6
  • Aliases:
    • NS6
Homo sapiens (human)
DOID:4549
  • extraskeletal myxoid chondrosarcoma
  • Aliases:
    • Myxoid extraosseous chondrosarcoma
    • extraosseous chondrosarcoma
Homo sapiens (human)
DOID:0060855
  • autosomal dominant pseudohypoaldosteronism type 1
  • Aliases:
    • PHA1A
    • autosomal dominant PHA 1
Homo sapiens (human)
DOID:0080943
  • 46,XX sex reversal 5
Homo sapiens (human)
DOID:0090059
  • enhanced S-cone syndrome
Homo sapiens (human)
DOID:0110399
  • retinitis pigmentosa 37
  • Aliases:
    • RP37
Homo sapiens (human)
DOID:0080156
  • X-linked adrenal hypoplasia congenita
  • Aliases:
    • congenital adrenal hypoplasia
Homo sapiens (human)
DOID:0111777
  • 46,XY sex reversal 2
  • Aliases:
    • 46,XY sex reversal, DAX1-related
    • 46XY sex reversal 2, dosage-sensitive
    • SRXY2
    • dosage-sensitive sex reversal
Homo sapiens (human)
DOID:2978
  • carbohydrate metabolic disorder
  • Aliases:
    • disorder of carbohydrate transport and metabolism
    • inborn carbohydrate metabolism disorder
    • inborn errors of carbohydrate metabolism
Saccharomyces cerevisiae S288C
DOID:0070316
  • Miura type epiphyseal chondrodysplasia
  • Aliases:
    • ECDM
    • tall stature-scoliosis-macrodactyly of the great toes syndrome
    • tall stature-scoliosis-macrodactyly of the halluces syndrome
Homo sapiens (human)
DOID:0080050
  • acromesomelic dysplasia, Maroteaux type
  • Aliases:
    • acromesomelic dysplasia-1
Homo sapiens (human)
DOID:11516
  • hypertensive heart disease
Homo sapiens (human)
DOID:0080663
  • atrial standstill 2
Homo sapiens (human)
DOID:13207
  • proliferative diabetic retinopathy
  • Aliases:
    • PDR
Saccharomyces cerevisiae S288C
DOID:0080333
  • aortic valve disease 1
Saccharomyces cerevisiae S288C
DOID:0060887
  • ossification of the posterior longitudinal ligament of spine
  • Aliases:
    • OPLL
Saccharomyces cerevisiae S288C
DOID:10754
  • otitis media
Saccharomyces cerevisiae S288C
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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