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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 January 28, 2025
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 1051 - 1075 of 5716 in total
Disease ID ▲ Disease Name Gene Symbol Gene ID Organism Source
DOID:0070151
  • hereditary sensory and autonomic neuropathy type 6
  • Aliases:
    • HSAN6
    • hereditary sensory and autonomic neuropathy type VI
Mus musculus (house mouse)
DOID:0070152
  • hereditary sensory and autonomic neuropathy type 1A
  • Aliases:
    • HSAN1A
    • hereditary sensory and autonomic neuropathy type IA
Homo sapiens (human)
DOID:0070154
  • hereditary sensory neuropathy type 1F
  • Aliases:
    • HSN1F
    • hereditary sensory neuropathy type IF
Homo sapiens (human)
DOID:0070155
  • hereditary sensory and autonomic neuropathy type 2A
  • Aliases:
    • HSAN2A
    • hereditary sensory and autonomic neuropathy type IIA
Homo sapiens (human)
DOID:0070157
  • hereditary sensory and autonomic neuropathy type 1C
  • Aliases:
    • HSAN1C
    • hereditary sensory and autonomic neuropathy type IC
Homo sapiens (human)
DOID:0070158
  • hereditary sensory neuropathy type 1E
  • Aliases:
    • HSN1E
    • hereditary sensory neuropathy type IE
Homo sapiens (human)
DOID:0070164
  • spermatogenic failure 2
  • Aliases:
    • SPGF2
Homo sapiens (human)
DOID:0070165
  • spermatogenic failure 18
  • Aliases:
    • SPGF18
Homo sapiens (human)
DOID:0070166
  • spermatogenic failure 20
  • Aliases:
    • SPGF20
Homo sapiens (human)
DOID:0070168
  • spermatogenic failure 3
  • Aliases:
    • SPGF3
Homo sapiens (human)
DOID:0070170
  • spermatogenic failure 19
  • Aliases:
    • SPGF19
Homo sapiens (human)
DOID:0070174
  • spermatogenic failure 17
  • Aliases:
    • Male infertility due to oocyte activation failure
    • SPGF17
Homo sapiens (human)
DOID:0070177
  • spermatogenic failure 22
  • Aliases:
    • SPGF22
Homo sapiens (human)
DOID:0070182
  • spermatogenic failure 13
  • Aliases:
    • SPGF13
Homo sapiens (human)
DOID:0070187
  • Y-linked spermatogenic failure 2
  • Aliases:
    • SPGFY2
    • nonobstructive Y-linked spermatogenic failure
Homo sapiens (human)
DOID:0070195
  • X-linked chronic granulomatous disease
  • Aliases:
    • CDGX
    • X-linked chronic cytochrome b-negative granulomatous disease
Homo sapiens (human)
DOID:0070197
  • distal myopathy 1
  • Aliases:
    • Distal myopathy type 1
    • Gowers disease
    • Laing distal myopathy
    • Laing early-onset distal myopathy
    • MPD1
Homo sapiens (human)
DOID:0070199
  • Miyoshi muscular dystrophy 1
  • Aliases:
    • MMD1
    • Miyoshi myopathy 1
Homo sapiens (human)
DOID:0070201
  • Miyoshi muscular dystrophy 3
  • Aliases:
    • MMD3
    • Miyoshi myopathy 3
Homo sapiens (human)
DOID:0070202
  • familial partial lipodystrophy type 2
  • Aliases:
    • FPLD2
    • familial lipodystrophy of limbs and lower trunk
    • familial partial lipodystrophy Dunnigan type
    • reverse partial lipodystrophy
Homo sapiens (human)
DOID:0070204
  • familial partial lipodystrophy type 3
  • Aliases:
    • FPLD3
    • PPARG-related FPLD
    • PPARG-related familial partial lipodystrophy
    • familial partial lipodystrophy associated with PPARG mutations
Homo sapiens (human)
DOID:0070205
  • familial partial lipodystrophy type 4
  • Aliases:
    • FPLD4
    • PLIN1-related FPLD
    • PLIN1-related familial partial lipodystrophy
    • familial partial lipodystrophy associated with PLIN1 mutations
Homo sapiens (human)
DOID:0070208
  • hereditary lymphedema IC
  • Aliases:
    • LMPH1C
Homo sapiens (human)
DOID:0070209
  • hereditary lymphedema ID
  • Aliases:
    • LMPH1D
Homo sapiens (human)
DOID:0070210
  • hereditary lymphedema IA
  • Aliases:
    • LMPH1A
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 8, 2025