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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 7426 - 7450 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:5200
  • urinary tract obstruction
  • Aliases:
    • Obstructive Uropathy
    • urinary obstruction
Homo sapiens (human)
DOID:480
  • movement disease
Homo sapiens (human)
DOID:0070072
  • autosomal dominant intellectual developmental disorder 42
  • Aliases:
    • MRD42
    • autosomal dominant mental retardation 42
    • autosomal dominant non-syndromic intellectual disability 42
Homo sapiens (human)
DOID:0110542
  • autosomal dominant nonsyndromic deafness 10
  • Aliases:
    • DFNA10
    • autosomal dominant deafness 10
Homo sapiens (human)
DOID:0050083
  • Keshan disease
Homo sapiens (human)
DOID:0050637
  • Finnish type amyloidosis
  • Aliases:
    • AGel amyloidosis
    • AMYLOIDOSIS, MERETOJA TYPE
    • Lattice corneal dystrophy type II
    • gelsolin amyloidosis
Homo sapiens (human)
DOID:0111861
  • Meester-Loeys syndrome
  • Aliases:
    • MRLS
Homo sapiens (human)
DOID:0111051
  • platelet-type bleeding disorder 18
  • Aliases:
    • BDPLT18
    • bleeding disorder due to CalDAG-GEFI deficiency
    • bleeding disorder due to calcium- and DAG-regulated guanine exchange factor-1 deficiency
Homo sapiens (human)
DOID:0060772
  • multiple types of congenital heart defects 6
  • Aliases:
    • DTGA3
    • dextro-looped transposition of the great arteries 3
Homo sapiens (human)
DOID:0070343
  • CSF1R-related brain malformation and osteopetrosis
  • Aliases:
    • osteoporosis and infantile neuroaxonal dystrophy
Homo sapiens (human)
DOID:0060278
  • pontocerebellar hypoplasia type 9
Homo sapiens (human)
DOID:0080799
  • sinonasal undifferentiated carcinoma
Homo sapiens (human)
DOID:4186
  • articulation disorder
  • Aliases:
    • Articulation impairment
    • Phonological disorder
Homo sapiens (human)
DOID:0070165
  • spermatogenic failure 18
  • Aliases:
    • SPGF18
Homo sapiens (human)
DOID:0080136
  • multiple mitochondrial dysfunctions syndrome 4
Homo sapiens (human)
DOID:0111962
  • combined immunodeficiency
Homo sapiens (human)
DOID:0111837
  • congenital nongoitrous hypothyroidism 8
  • Aliases:
    • CHNG8
Homo sapiens (human)
DOID:0110336
  • osteogenesis imperfecta type 8
  • Aliases:
    • OI8
    • osteogenesis imperfecta type VIII
Homo sapiens (human)
DOID:14219
  • renal tubular acidosis
Homo sapiens (human)
DOID:3911
  • progeria
  • Aliases:
    • HGPS
    • Hutchinson Gilford syndrome
    • Hutchinson-Gilford Progeria syndrome
    • Hutchinson-Gilford disease
Homo sapiens (human)
DOID:6364
  • migraine
  • Aliases:
    • migraine disorder
    • migraine variant
    • migraine with or without aura
Homo sapiens (human)
DOID:0090135
  • complex cortical dysplasia with other brain malformations 5
  • Aliases:
    • CDCBM5
Homo sapiens (human)
DOID:10881
  • hand, foot and mouth disease
  • Aliases:
    • Vesicular stomatitis and exanthem
Homo sapiens (human)
DOID:0060264
  • pontocerebellar hypoplasia
  • Aliases:
    • PCH
Homo sapiens (human)
DOID:0111735
  • X-linked deafness 4
  • Aliases:
    • DFN6
    • DFNX4
    • X-linked progressive deafness 6
    • nonsyndromic sensorineural progressive deafness 6
Homo sapiens (human)
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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