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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 **9801 - 9825** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism	Source
DOID:0080493	ovarian dysgenesis 1	FSHR	2492	Homo sapiens (human)	Alliance of Genome Resources
DOID:14450	46 XX gonadal dysgenesis Aliases: ovarian dysgenesis	FSHR NUP107	2492 57122	Homo sapiens (human)	Alliance of Genome Resources
DOID:13938	amenorrhea Aliases: absence of menstruation amenia	FSHB	2488	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090088	hypogonadotropic hypogonadism 24 without anosmia Aliases: isolated follicle-stimulating hormone deficiency	FSHB	2488	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112018	non-syndromic X-linked intellectual disability 104 Aliases: MRX104 X-linked mental retardation 104	FRMPD4	9758	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111717	isolated cryptophthalmia Aliases: CRYPTOP unilateral or bilateral isolated cryptophthalmos	FREM2	341640	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111407	Fraser syndrome 2 Aliases: FRASRS2	FREM2	341640	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060732	chromosome 9p deletion syndrome Aliases: 9p syndrome Alfi syndrome monosomy 9p syndrome	FREM1	158326	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111405	Fraser syndrome 1 Aliases: FRASRS1	FRAS1	80144	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090001	Fraser syndrome Aliases: cryptophthalmos with other malformations	FRAS1 FREM1 FREM2 GRIP1	158326 23426 341640 80144	Homo sapiens (human)	Alliance of Genome Resources
DOID:4724	brain edema Aliases: intracranial swelling wet brain	FPS1	850683	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0111275	speech-language disorder-1 Aliases: CAS articulatory apraxia childhood apraxia of speech developmental apraxia of speech developmental verbal dyspraxia speech and language disorder with orofacial dyspraxia speech-language disorder type 1	FOXP2	93986	Homo sapiens (human)	Alliance of Genome Resources
DOID:93	language disorder	FOXP2	93986	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111331	intellectual disability-severe speech delay-mild dysmorphism syndrome Aliases: FOXP1 Haploinsufficiency FOXP1 syndrome FOXP1-Related Neurodevelopmental Disorder Mental retardation with language impairment and with or without autistic features	FOXP1	27086	Homo sapiens (human)	Alliance of Genome Resources
DOID:1255	trichostrongyloidiasis	FOXP1	27086	Homo sapiens (human)	Alliance of Genome Resources
DOID:5117	dermoid cyst of ovary Aliases: Dermoid cyst Ovarian Dermoid Cyst	FOXO3	2309	Homo sapiens (human)	Alliance of Genome Resources
DOID:4051	alveolar rhabdomyosarcoma Aliases: alveolar childhood rhabdomyosarcoma	FOXO1	2308	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080860	primary ovarian insufficiency 3	FOXL2	668	Homo sapiens (human)	Alliance of Genome Resources
DOID:14778	blepharophimosis, ptosis, and epicanthus inversus syndrome	FOXL2	668	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060341	agnathia-otocephaly complex Aliases: agnathia-holoprosencephaly-situs inversus syndrome dysgnathia complex agnathia-holoprosencephaly holoprosencephaly-agnathia otocephaly	FOXH1	8928	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080608	anterior segment dysgenesis 3	FOXC1	2296	Homo sapiens (human)	Alliance of Genome Resources
DOID:14686	Axenfeld-Rieger syndrome Aliases: Anomaly, Rieger's Axenfeld syndrome RGS - Rieger syndrome Rieger's anomaly	FOXC1 PITX2	2296 5308	Homo sapiens (human)	Alliance of Genome Resources
DOID:4451	renal carcinoma Aliases: carcinoma of kidney kidney carcinoma	FOSL2 JUN JUNB JUND	2355 3725 3726 3727	Homo sapiens (human)	Alliance of Genome Resources
DOID:11371	functional diarrhea Aliases: functional diarrhoea	FOS	2353	Homo sapiens (human)	Alliance of Genome Resources
DOID:2384	Wernicke encephalopathy Aliases: Wernicke's disease Wernicke's encephalopathy	FOS PTGS2	2353 5743	Homo sapiens (human)	Alliance of Genome Resources

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