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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 15551 - 15575 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:0050876
  • Caroli disease
Homo sapiens (human)
DOID:0050876
  • Caroli disease
Rattus norvegicus (Norway rat)
DOID:0050876
  • Caroli disease
Caenorhabditis elegans
DOID:0080533
  • Carney-Stratakis syndrome
Mus musculus (house mouse)
DOID:0080533
  • Carney-Stratakis syndrome
Homo sapiens (human)
DOID:0080533
  • Carney-Stratakis syndrome
Rattus norvegicus (Norway rat)
DOID:0050471
  • Carney complex
  • Aliases:
    • Carney Complex, Type 1
    • Carney Complex, Type 2
    • Carney Syndrome
    • Carney complex variant
    • LAMB Syndrome
    • NAME Syndrome
Homo sapiens (human)
DOID:3613
  • Canavan disease
  • Aliases:
    • ACY2 DEFICIENCY
    • AMINOACYLASE 2 DEFICIENCY
    • ASP DEFICIENCY
    • ASPA DEFICIENCY
    • ASPARTOACYLASE DEFICIENCY
    • CANAVAN-VAN BOGAERT-BERTRAND DISEASE
    • Spongy degeneration of central nervous system
Homo sapiens (human)
DOID:3613
  • Canavan disease
  • Aliases:
    • ACY2 DEFICIENCY
    • AMINOACYLASE 2 DEFICIENCY
    • ASP DEFICIENCY
    • ASPA DEFICIENCY
    • ASPARTOACYLASE DEFICIENCY
    • CANAVAN-VAN BOGAERT-BERTRAND DISEASE
    • Spongy degeneration of central nervous system
Rattus norvegicus (Norway rat)
DOID:3613
  • Canavan disease
  • Aliases:
    • ACY2 DEFICIENCY
    • AMINOACYLASE 2 DEFICIENCY
    • ASP DEFICIENCY
    • ASPA DEFICIENCY
    • ASPARTOACYLASE DEFICIENCY
    • CANAVAN-VAN BOGAERT-BERTRAND DISEASE
    • Spongy degeneration of central nervous system
Mus musculus (house mouse)
DOID:4997
  • Camurati-Engelmann disease
  • Aliases:
    • Diaphyseal dysplasia
    • Engelman's disease
    • progressive diaphyseal dysplasia
Rattus norvegicus (Norway rat)
DOID:4997
  • Camurati-Engelmann disease
  • Aliases:
    • Diaphyseal dysplasia
    • Engelman's disease
    • progressive diaphyseal dysplasia
Mus musculus (house mouse)
DOID:4997
  • Camurati-Engelmann disease
  • Aliases:
    • Diaphyseal dysplasia
    • Engelman's disease
    • progressive diaphyseal dysplasia
Xenopus laevis (African clawed frog)
DOID:4997
  • Camurati-Engelmann disease
  • Aliases:
    • Diaphyseal dysplasia
    • Engelman's disease
    • progressive diaphyseal dysplasia
Homo sapiens (human)
DOID:4257
  • Caffey disease
  • Aliases:
    • cortical congenital hyperostosis
    • infantile cortical hyperostosis
Mus musculus (house mouse)
DOID:4257
  • Caffey disease
  • Aliases:
    • cortical congenital hyperostosis
    • infantile cortical hyperostosis
Homo sapiens (human)
DOID:4257
  • Caffey disease
  • Aliases:
    • cortical congenital hyperostosis
    • infantile cortical hyperostosis
Rattus norvegicus (Norway rat)
DOID:0070027
  • CST3-related cerebral amyloid angiopathy
  • Aliases:
    • Amyloidosis VI
    • Amyloidosis, Cerebroarterial, Icelandic Type
    • Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant
    • HCHWA
    • Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant
Caenorhabditis elegans
DOID:0070027
  • CST3-related cerebral amyloid angiopathy
  • Aliases:
    • Amyloidosis VI
    • Amyloidosis, Cerebroarterial, Icelandic Type
    • Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant
    • HCHWA
    • Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant
Mus musculus (house mouse)
DOID:0070027
  • CST3-related cerebral amyloid angiopathy
  • Aliases:
    • Amyloidosis VI
    • Amyloidosis, Cerebroarterial, Icelandic Type
    • Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant
    • HCHWA
    • Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant
Rattus norvegicus (Norway rat)
DOID:0070343
  • CSF1R-related brain malformation and osteopetrosis
  • Aliases:
    • osteoporosis and infantile neuroaxonal dystrophy
Mus musculus (house mouse)
DOID:0070343
  • CSF1R-related brain malformation and osteopetrosis
  • Aliases:
    • osteoporosis and infantile neuroaxonal dystrophy
Homo sapiens (human)
DOID:0070343
  • CSF1R-related brain malformation and osteopetrosis
  • Aliases:
    • osteoporosis and infantile neuroaxonal dystrophy
Caenorhabditis elegans
DOID:0070343
  • CSF1R-related brain malformation and osteopetrosis
  • Aliases:
    • osteoporosis and infantile neuroaxonal dystrophy
Danio rerio (zebrafish)
DOID:0060218
  • CREST syndrome
Mus musculus (house mouse)
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Last updated: December 9, 2024