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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 3901 - 3925 of 15957 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲ Source
DOID:0110975
  • brachydactyly type B2
  • Aliases:
    • BDB2
Homo sapiens (human)
DOID:11123
  • Henoch-Schoenlein purpura
  • Aliases:
    • Allergic purpura
    • Autoimmune purpura
    • Henoch-Sch?nlein purpura
    • Henoch-Sch@nlein purpura
    • Henoch-Scholein purpura
    • Henoch-Schonlein Purpura
    • Purpura, autoimmune
Homo sapiens (human)
DOID:0080137
  • multiple endocrine neoplasia type 4
  • Aliases:
    • Multiple Endocrine Neoplasia, Type IV
Homo sapiens (human)
DOID:0110356
  • retinitis pigmentosa 18
  • Aliases:
    • RP18
Homo sapiens (human)
DOID:0080773
  • delta beta-thalassemia
Homo sapiens (human)
DOID:12835
  • quadriplegia
  • Aliases:
    • tetraplegia
Homo sapiens (human)
DOID:0090032
  • Silverman-Handmaker type dyssegmental dysplasia
Homo sapiens (human)
DOID:0060835
  • isolated microphthalmia 6
  • Aliases:
    • MCOP6
    • posterior nonsyndromic microphthalmia
Homo sapiens (human)
DOID:0110617
  • primary ciliary dyskinesia 5
  • Aliases:
    • CILD5
    • primary ciliary dyskinesia 5 without situs inversus
Homo sapiens (human)
DOID:0080521
  • lung non-squamous non-small cell carcinoma
  • Aliases:
    • non- squamous NSCLC
Homo sapiens (human)
DOID:0070329
  • mitochondrial DNA depletion syndrome
  • Aliases:
    • mtDNA depletion syndrome
Homo sapiens (human)
DOID:0111578
  • Gillespie syndrome
  • Aliases:
    • GLSP
    • aniridia, cerebellar ataxia and mental deficiency
    • aniridia-cerebellar ataxia-intellectual disability syndrome
Homo sapiens (human)
DOID:0111545
  • familial male-limited precocious puberty
  • Aliases:
    • FMPP
    • familial gonadotropin-independent male-limited sexual precocity
    • male-limited precocious puberty
    • testotoxicosis
Homo sapiens (human)
DOID:0090114
  • Sorsby's fundus dystrophy
  • Aliases:
    • SFD
    • hemorrhagic macular dystrophy
    • pseudoinflammatory fundus dystrophy of Sorsby
Homo sapiens (human)
DOID:3114
  • serous cystadenocarcinoma
  • Aliases:
    • serous adenocarcinoma
    • serous carcinoma
Homo sapiens (human)
DOID:0080384
  • nephrotic syndrome type 6
Homo sapiens (human)
DOID:9562
  • primary ciliary dyskinesia
  • Aliases:
    • ciliary motility disorder
    • immotile ciliary syndrome
Homo sapiens (human)
DOID:5940
  • malignant peripheral nerve sheath tumor
  • Aliases:
    • malignant neoplasm of the peripheral nerve Sheath
Homo sapiens (human)
DOID:4648
  • familial retinoblastoma
  • Aliases:
    • Hereditary Retinoblastoma
Homo sapiens (human)
DOID:0060748
  • familial temporal lobe epilepsy 1
  • Aliases:
    • ETL1
    • partial epilepsy with auditory features
Homo sapiens (human)
DOID:399
  • tuberculosis
Homo sapiens (human)
DOID:3651
  • pyruvate carboxylase deficiency disease
  • Aliases:
    • deficiency of pyruvic carboxylase
Homo sapiens (human)
DOID:0112133
  • severe congenital neutropenia 3
  • Aliases:
    • Kostmann disease
    • Kostmann syndrome
    • SCN3
    • infantile agranulocytosis
Homo sapiens (human)
DOID:0050873
  • follicular lymphoma
Homo sapiens (human)
DOID:18
  • urinary system disease
  • Aliases:
    • Non-neoplastic urinary tract disease
    • urinary tract disease
Homo sapiens (human)
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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