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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 15026 - 15050 of 15957 in total
Disease ID Disease Name ▼ Gene Symbol Gene ID Organism Source
DOID:0111405
  • Fraser syndrome 1
  • Aliases:
    • FRASRS1
Homo sapiens (human)
DOID:0111405
  • Fraser syndrome 1
  • Aliases:
    • FRASRS1
Mus musculus (house mouse)
DOID:0111789
  • Frank-Ter Haar syndrome
  • Aliases:
    • Borrone dermatocardioskeletal syndrome
    • FTHS
    • Ter Haar syndrome
    • autosomal recessive Melnick-Needles syndrome
    • megalocornea, multiple skeletal anomalies, and developmental delay
Homo sapiens (human)
DOID:0111789
  • Frank-Ter Haar syndrome
  • Aliases:
    • Borrone dermatocardioskeletal syndrome
    • FTHS
    • Ter Haar syndrome
    • autosomal recessive Melnick-Needles syndrome
    • megalocornea, multiple skeletal anomalies, and developmental delay
Mus musculus (house mouse)
DOID:0111358
  • Floating-Harbor syndrome
  • Aliases:
    • FLHS
Homo sapiens (human)
DOID:0060448
  • Fleck corneal dystrophy
  • Aliases:
    • FCD
    • Francois-Neetens speckled corneal dystrophy
Saccharomyces cerevisiae S288C
DOID:0060448
  • Fleck corneal dystrophy
  • Aliases:
    • FCD
    • Francois-Neetens speckled corneal dystrophy
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:0050637
  • Finnish type amyloidosis
  • Aliases:
    • AGel amyloidosis
    • AMYLOIDOSIS, MERETOJA TYPE
    • Lattice corneal dystrophy type II
    • gelsolin amyloidosis
Mus musculus (house mouse)
DOID:0112194
  • Filippi syndrome
  • Aliases:
    • Scott craniodigital syndrome with mental retardation
    • type 1 syndactyly-microcephaly-intellectual disability syndrome
Mus musculus (house mouse)
DOID:0112194
  • Filippi syndrome
  • Aliases:
    • Scott craniodigital syndrome with mental retardation
    • type 1 syndactyly-microcephaly-intellectual disability syndrome
Homo sapiens (human)
DOID:5585
  • Ferguson-Smith tumor
  • Aliases:
    • Multiple self-healing epithelioma of Ferguson-Smith
Homo sapiens (human)
DOID:5585
  • Ferguson-Smith tumor
  • Aliases:
    • Multiple self-healing epithelioma of Ferguson-Smith
Rattus norvegicus (Norway rat)
DOID:5585
  • Ferguson-Smith tumor
  • Aliases:
    • Multiple self-healing epithelioma of Ferguson-Smith
Mus musculus (house mouse)
DOID:5585
  • Ferguson-Smith tumor
  • Aliases:
    • Multiple self-healing epithelioma of Ferguson-Smith
Caenorhabditis elegans
DOID:0060464
  • Feingold syndrome
  • Aliases:
    • FGLDS
    • MODED syndrome
    • ODED syndrome
    • digital anomalies with short palpebral fissures and atresia of esophagus or duodenum
    • microcephaly-digital anomalies-normal intelligence syndrome
    • microcephaly-oculo-digito-esophageal-duodenal syndrome
    • oculo-digito-esophageal-duodenal syndrome
Mus musculus (house mouse)
DOID:0060464
  • Feingold syndrome
  • Aliases:
    • FGLDS
    • MODED syndrome
    • ODED syndrome
    • digital anomalies with short palpebral fissures and atresia of esophagus or duodenum
    • microcephaly-digital anomalies-normal intelligence syndrome
    • microcephaly-oculo-digito-esophageal-duodenal syndrome
    • oculo-digito-esophageal-duodenal syndrome
Homo sapiens (human)
DOID:0080632
  • Fazio-Londe disease
  • Aliases:
    • riboflavin transporter deficiency neuronopathy
Caenorhabditis elegans
DOID:0080632
  • Fazio-Londe disease
  • Aliases:
    • riboflavin transporter deficiency neuronopathy
Mus musculus (house mouse)
DOID:0080632
  • Fazio-Londe disease
  • Aliases:
    • riboflavin transporter deficiency neuronopathy
Homo sapiens (human)
DOID:0080632
  • Fazio-Londe disease
  • Aliases:
    • riboflavin transporter deficiency neuronopathy
Rattus norvegicus (Norway rat)
DOID:0080632
  • Fazio-Londe disease
  • Aliases:
    • riboflavin transporter deficiency neuronopathy
Danio rerio (zebrafish)
DOID:0050464
  • Farber lipogranulomatosis
  • Aliases:
    • Farber disease
    • N-laurylsphingosine deacylase deficiency
    • acid ceramidase deficiency
Homo sapiens (human)
DOID:0050464
  • Farber lipogranulomatosis
  • Aliases:
    • Farber disease
    • N-laurylsphingosine deacylase deficiency
    • acid ceramidase deficiency
Rattus norvegicus (Norway rat)
DOID:0050464
  • Farber lipogranulomatosis
  • Aliases:
    • Farber disease
    • N-laurylsphingosine deacylase deficiency
    • acid ceramidase deficiency
Caenorhabditis elegans
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Last updated: December 9, 2024