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 July 29, 2024
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 2876 - 2900 of 4621 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Organism
DOID:0090089
  • hypogonadotropic hypogonadism 10 with or without anosmia
Homo sapiens (human)
DOID:0090083
  • hypogonadotropic hypogonadism 2 with or without anosmia
Homo sapiens (human)
DOID:0090085
  • hypogonadotropic hypogonadism 9 with or without anosmia
Homo sapiens (human)
DOID:0090080
  • hypogonadotropic hypogonadism 16 with or without anosmia
Homo sapiens (human)
DOID:0090077
  • hypogonadotropic hypogonadism 4 with or without anosmia
Homo sapiens (human)
DOID:0090082
  • hypogonadotropic hypogonadism 20 with or without anosmia
Homo sapiens (human)
DOID:0090084
  • hypogonadotropic hypogonadism 5 with or without anosmia
Homo sapiens (human)
DOID:0090087
  • hypogonadotropic hypogonadism 14 with or without anosmia
Homo sapiens (human)
DOID:0060874
  • isolated growth hormone deficiency type IB
  • Aliases:
    • IGHD IB
    • congenital IGHD type IB
    • congenital isolated GH deficiency type IB
    • congenital isolated growth hormone deficiency type IB
    • dwarfism of Sindh
Homo sapiens (human)
DOID:9406
  • hypopituitarism
  • Aliases:
    • Pituitary insufficiency
    • pituitary hormone deficiency
Homo sapiens (human)
DOID:0090076
  • hypogonadotropic hypogonadism 18 with or without anosmia
Homo sapiens (human)
DOID:0060875
  • isolated growth hormone deficiency type III
  • Aliases:
    • Fleisher syndrome
    • IGHD III
    • X-linked IGHD
    • X-linked agammaglobulinemia and isolated growth hormone deficiency
    • X-linked hypogammaglobulinemia and isolated growth hormone deficiency
    • X-linked isolated growth hormone deficiency
    • congenital IGHD type III
    • congenital isolated GH deficiency type III
    • congenital isolated growth hormone deficiency type III
    • growth hormone deficiency with hypogammaglobulinemia
Homo sapiens (human)
DOID:0090081
  • hypogonadotropic hypogonadism 22 with or without anosmia
Homo sapiens (human)
DOID:0060872
  • isolated growth hormone deficiency type II
  • Aliases:
    • IGHD II
    • autosomal dominant isolated growth hormone deficiency
    • autosomal dominant pituitary dwarfism due to isolated growth hormone deficiency
    • congenital IGHD type II
    • congenital isolated GH deficiency type II
    • congenital isolated growth hormone deficiency type II
Homo sapiens (human)
DOID:9410
  • panhypopituitarism
  • Aliases:
    • Simmond's disease
    • Simmonds' disease
    • combined pituitary hormone deficiency
Homo sapiens (human)
DOID:0090074
  • hypogonadotropic hypogonadism 8 with or without anosmia
Homo sapiens (human)
DOID:0090090
  • hypogonadotropic hypogonadism 19 with or without anosmia
Homo sapiens (human)
DOID:9476
  • Sheehan syndrome
  • Aliases:
    • Postpartum Hypopituitarism
    • Sheehan's syndrome
Homo sapiens (human)
DOID:0090086
  • hypogonadotropic hypogonadism 6 with or without anosmia
Homo sapiens (human)
DOID:0090070
  • hypogonadotropic hypogonadism
  • Aliases:
    • congenital idiopathic hypogonadotropic hypogonadism
    • hypogonadotropism
    • isolated congenital gonadotropin deficiency
Homo sapiens (human)
DOID:0090092
  • hypogonadotropic hypogonadism 3 with or without anosmia
Homo sapiens (human)
DOID:0090073
  • hypogonadotropic hypogonadism 13 with or without anosmia
Homo sapiens (human)
DOID:0090093
  • hypogonadotropic hypogonadism 21 with or without anosmia
Homo sapiens (human)
DOID:0090094
  • hypogonadotropic hypogonadism 1 with or without anosmia
  • Aliases:
    • dysplasia olfactogenitalis of de morsier
Homo sapiens (human)
DOID:3614
  • Kallmann syndrome
  • Aliases:
    • Hypogonadism with anosmia
    • Kallman syndrome
    • Kallman's syndrome
    • familial hypogonadism with anosmia
Homo sapiens (human)

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024