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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 6901 - 6925 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:0111133
  • focal segmental glomerulosclerosis 8
  • Aliases:
    • FSGS8
Homo sapiens (human)
DOID:0111448
  • progressive myoclonus epilepsy 1B
  • Aliases:
    • EPM1B
Homo sapiens (human)
DOID:0050117
  • disease by infectious agent
  • Aliases:
    • infectious disease
Homo sapiens (human)
DOID:0110725
  • neuronal ceroid lipofuscinosis 10
  • Aliases:
    • CLN10
    • Cathepsin D deficiency
    • neuronal ceroid lipofuscinosis cathepsin D-deficient
    • neuronal ceroid lipofuscinosis due to cathepsin D deficiency
Homo sapiens (human)
DOID:0050464
  • Farber lipogranulomatosis
  • Aliases:
    • Farber disease
    • N-laurylsphingosine deacylase deficiency
    • acid ceramidase deficiency
Homo sapiens (human)
DOID:0050539
  • Charcot-Marie-Tooth disease type 2
  • Aliases:
    • hereditary motor and sensory neuropathy Guadalajara neuronal type
    • hereditary motor and sensory neuropathy Okinawa type
    • hereditary motor and sensory neuropathy type 2
Homo sapiens (human)
DOID:14415
  • Legg-Calve-Perthes disease
  • Aliases:
    • Calve - Perthes' disease
    • Coxa plana
    • Juvenile osteochond-hip/pelvis
    • Juvenile osteochondrosis of hip and/or pelvis
    • Perthe's disease
    • Perthes disease
    • juvenile osteochondrosis of hip and pelvis
    • osteochondrosis of Legg-Calve-Perthes
    • pseudocoxalgia
Homo sapiens (human)
DOID:0081290
  • Antley-Bixler syndrome without disordered steroidogenesis
Homo sapiens (human)
DOID:0060597
  • atypical chronic myeloid leukemia, BCR-ABL1 negative
  • Aliases:
    • aCML
    • atypical CML
    • atypical chronic myeloid leukaemia
    • atypical chronic myeloid leukaemia BCR-ABL1 negative
    • atypical chronic myeloid leukemia BCR-ABL1 negative
    • subacute myeloid leukemia
Homo sapiens (human)
DOID:0081352
  • congenital myopathy 20
Homo sapiens (human)
DOID:0111583
  • carboxypeptidase N deficiency
  • Aliases:
    • anaphylotoxin inactivator deficiency
    • deficiency of carboxypeptidase B
Homo sapiens (human)
DOID:0060250
  • idiopathic scoliosis
Homo sapiens (human)
DOID:4325
  • Ebola hemorrhagic fever
  • Aliases:
    • Ebola virus disease
Homo sapiens (human)
DOID:0111682
  • diffuse cystic renal dysplasia
  • Aliases:
    • CYSRD
    • renal dysplasia diffuse cystic
    • susceptibility to cystic renal dysplasia
Homo sapiens (human)
DOID:0110176
  • Charcot-Marie-Tooth disease axonal type 2X
  • Aliases:
    • Charcot-Marie-Tooth neuropathy type 2X
    • autosomal recessive axonal Charcot-Marie-Tooth disease type 2X
Homo sapiens (human)
DOID:0060933
  • developmental delay, dysmorphic facies, and brain anomalies
  • Aliases:
    • DEVDFB
Homo sapiens (human)
DOID:3192
  • neurilemmoma
  • Aliases:
    • Psammomatous schwannoma
    • schwannoma
Homo sapiens (human)
DOID:823
  • periapical periodontitis
  • Aliases:
    • Apical periodontitis
Homo sapiens (human)
DOID:0060569
  • hypertrichotic osteochondrodysplasia Cantu type
  • Aliases:
    • Cantu syndrome
Homo sapiens (human)
DOID:219
  • colon cancer
Homo sapiens (human)
DOID:0111292
  • idiopathic generalized epilepsy 10
  • Aliases:
    • EIG10
Homo sapiens (human)
DOID:13976
  • peptic esophagitis
  • Aliases:
    • Peptic reflux disease
    • Reflux oesophagitis
    • reflux esophagitis
Homo sapiens (human)
DOID:0110074
  • arrhythmogenic right ventricular dysplasia 5
  • Aliases:
    • ARVC5
    • ARVD5
    • arrhythmogenic right ventricular cardiomyopathy 5
    • familial arrhythmogenic right ventricular dysplasia 5
Homo sapiens (human)
DOID:0050547
  • familial medullary thyroid carcinoma
  • Aliases:
    • THYROID CARCINOMA, FAMILIAL MEDULLARY
Homo sapiens (human)
DOID:0050759
  • myotonic dystrophy type 2
Homo sapiens (human)
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Last updated: December 9, 2024