GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source Last Updated
Alliance of Genome Resources July 29, 2024
DisGeNET July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 2351 - 2375 of 7942 in total
Disease ID Disease Name Gene Symbol Gene ID Organism ▲
DOID:9974
  • drug dependence
Homo sapiens (human)
DOID:7689
  • leptomeninges sarcoma
  • Aliases:
    • Leptomeningeal sarcoma
    • sarcoma of Leptomeninges
Homo sapiens (human)
DOID:0110534
  • autosomal recessive nonsyndromic deafness 89
  • Aliases:
    • DFNB89
    • autosomal recessive deafness 89
Homo sapiens (human)
DOID:2983
  • anuria
  • Aliases:
    • Suppression of urinary secretion
Homo sapiens (human)
DOID:14223
  • ochronosis
Homo sapiens (human)
DOID:12733
  • hypercementosis
  • Aliases:
    • Cementation hyperplasia
Homo sapiens (human)
DOID:0110423
  • dilated cardiomyopathy 1C
  • Aliases:
    • CMDC1
    • dilated cardiomyopathy 1C with or without left ventricular noncompaction
Homo sapiens (human)
DOID:5535
  • gallbladder squamous cell carcinoma
  • Aliases:
    • Epidermoid gallbladder carcinoma
Homo sapiens (human)
DOID:0060488
  • Pitt-Hopkins syndrome
Homo sapiens (human)
DOID:1724
  • duodenal ulcer
  • Aliases:
    • Curling Ulcer
    • Curling's ulcers
    • Stress Ulcer
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:0080342
  • Simpson-Golabi-Behmel syndrome type 2
Homo sapiens (human)
DOID:7997
  • thyrotoxicosis
Homo sapiens (human)
DOID:5608
  • dental pulp calcification
  • Aliases:
    • pulp calcification
    • pulp calcifications
    • pulpal calcifications
Homo sapiens (human)
DOID:381
  • arthropathy
  • Aliases:
    • Ankylosis of joint of ankle and/or foot
    • Ankylosis of joint of forearm
    • Ankylosis of joint of hand
    • Ankylosis of joint of lower leg
    • Ankylosis of joint of upper arm
    • Ankylosis of multiple joints
    • Infectious arthropathy
    • Joint ankylosis of the ankle and foot
    • Joint ankylosis of the ankle and/or foot
    • Joint ankylosis of the forearm
    • Joint ankylosis of the hand
    • Joint ankylosis of the lower leg
    • Joint ankylosis of the pelvic region and thigh
    • Joint ankylosis of the shoulder region
    • Joint ankylosis of the upper arm
    • ankylosis of ankle and foot joint
    • ankylosis of forearm joint
    • ankylosis of hand joint
    • ankylosis of joint of multiple sites
    • ankylosis of joint of pelvic region and thigh
    • ankylosis of joint of shoulder region
    • ankylosis of lower leg joint
    • ankylosis of upper arm joint
Homo sapiens (human)
DOID:5200
  • urinary tract obstruction
  • Aliases:
    • Obstructive Uropathy
    • urinary obstruction
Homo sapiens (human)
DOID:12577
  • urethral obstruction
  • Aliases:
    • Obstruction of urethra
Homo sapiens (human)
DOID:0110445
  • dilated cardiomyopathy 1KK
  • Aliases:
    • CMD1KK
Homo sapiens (human)
DOID:2513
  • basal cell carcinoma
  • Aliases:
    • Basal cell cancer
    • Basal cell carcinoma of skin
    • Basal cell neoplasm
    • Basal cell tumor
    • Epithelioma basal cell
    • Rodent ulcer
    • malignant Basal cell neoplasm
    • malignant basal cell tumor
Homo sapiens (human)
DOID:0110038
  • Alzheimer's disease 6
  • Aliases:
    • AD6
    • Alzheimer disease 6
    • Alzheimer disease 6, late onset
Homo sapiens (human)
DOID:0110163
  • Charcot-Marie-Tooth disease axonal type 2F
  • Aliases:
    • CMT2F
    • Charcot-Marie-Tooth neuronal type 2F
    • Charcot-Marie-Tooth neuropathy type 2F
    • autosomal dominant Charcot-Marie-Tooth disease type 2F
Homo sapiens (human)
DOID:0060873
  • isolated growth hormone deficiency type IA
  • Aliases:
    • IGHD IA
    • Illig-type growth hormone deficiency
    • autosomal recessive isolated growth hormone deficiency
    • pituitary dwarfism I
    • primordial dwarfism
    • sexual ateleiotic dwarfism
Homo sapiens (human)
DOID:2749
  • glycogen storage disease Ia
Homo sapiens (human)
DOID:0080216
  • duodenal atresia
Homo sapiens (human)
DOID:11211
  • buphthalmos
  • Aliases:
    • primary congenital glaucoma 3A
    • simple buphthalmos
Homo sapiens (human)

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Last updated: August 19, 2024