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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 **501 - 525** of **15957** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID	Organism	Source ▲
DOID:0050631	Allan-Herndon-Dudley syndrome Aliases: AHDS ALLAN-HERNDON SYNDROME	MCH4 MCH5	854030 854483	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0050632	oculocutaneous albinism	DCT OCA2 SLC45A2 TYR TYRP1	1638 4948 51151 7299 7306	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050632	oculocutaneous albinism	tyr-1	176105	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050632	oculocutaneous albinism	Dct Nsf Oca2 Slc45a2 Tyr Tyrp1	13190 18195 18431 22173 22178 22293	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050633	ocular albinism 1 Aliases: Albinism ocular 1 ocular albinism	tyr-1	176105	Caenorhabditis elegans	Alliance of Genome Resources
DOID:0050633	ocular albinism 1 Aliases: Albinism ocular 1 ocular albinism	GPR143 TYR	4935 7299	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050633	ocular albinism 1 Aliases: Albinism ocular 1 ocular albinism	Gpr143 Tyr	18241 22173	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050634	alopecia universalis Aliases: ALOPECIA UNIVERSALIS CONGENITA	Il4	287287	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050634	alopecia universalis Aliases: ALOPECIA UNIVERSALIS CONGENITA	IL4	3565	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050634	alopecia universalis Aliases: ALOPECIA UNIVERSALIS CONGENITA	Il4	16189	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050635	alternating hemiplegia of childhood Aliases: AHC	Atp1a2 Atp1a3	232975 98660	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050635	alternating hemiplegia of childhood Aliases: AHC	Atpalpha	48971	Drosophila melanogaster (fruit fly)	Alliance of Genome Resources
DOID:0050635	alternating hemiplegia of childhood Aliases: AHC	Atp1a2 Atp1a3	24212 24213	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050635	alternating hemiplegia of childhood Aliases: AHC	ATP1A2	477	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050636	familial visceral amyloidosis Aliases: AMYLOIDOSIS, FAMILIAL RENAL German type amyloidosis OSTERTAG TYPE AMYLOIDOSIS systemic nonneuropathic amyloidosis	Fga	14161	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050636	familial visceral amyloidosis Aliases: AMYLOIDOSIS, FAMILIAL RENAL German type amyloidosis OSTERTAG TYPE AMYLOIDOSIS systemic nonneuropathic amyloidosis	FGA	2243	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050637	Finnish type amyloidosis Aliases: AGel amyloidosis AMYLOIDOSIS, MERETOJA TYPE Lattice corneal dystrophy type II gelsolin amyloidosis	GSN	2934	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050637	Finnish type amyloidosis Aliases: AGel amyloidosis AMYLOIDOSIS, MERETOJA TYPE Lattice corneal dystrophy type II gelsolin amyloidosis	Gsn	227753	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050638	transthyretin amyloidosis Aliases: ATTR amyloidosis ATTRm amyloidosis Amyloidosis, hereditary, transthyretin-related Corino de Andrade's disease Familial transthyretin amyloidosis TTR amyloidosis familial amyloid polyneuropathy paramyloidosis transthyretin-related hereditary amyloidosis	Ttr	24856	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:0050638	transthyretin amyloidosis Aliases: ATTR amyloidosis ATTRm amyloidosis Amyloidosis, hereditary, transthyretin-related Corino de Andrade's disease Familial transthyretin amyloidosis TTR amyloidosis familial amyloid polyneuropathy paramyloidosis transthyretin-related hereditary amyloidosis	Ttr	22139	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050638	transthyretin amyloidosis Aliases: ATTR amyloidosis ATTRm amyloidosis Amyloidosis, hereditary, transthyretin-related Corino de Andrade's disease Familial transthyretin amyloidosis TTR amyloidosis familial amyloid polyneuropathy paramyloidosis transthyretin-related hereditary amyloidosis	TTR	7276	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050638	transthyretin amyloidosis Aliases: ATTR amyloidosis ATTRm amyloidosis Amyloidosis, hereditary, transthyretin-related Corino de Andrade's disease Familial transthyretin amyloidosis TTR amyloidosis familial amyloid polyneuropathy paramyloidosis transthyretin-related hereditary amyloidosis	ttr.L	397787	Xenopus laevis (African clawed frog)	Alliance of Genome Resources
DOID:0050639	primary cutaneous amyloidosis Aliases: PCA familial primary localized cutaneous amyloidosis	APOE	348	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050641	Rh deficiency syndrome	Rhag	19743	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0050641	Rh deficiency syndrome	Rhag	65207	Rattus norvegicus (Norway rat)	Alliance of Genome Resources

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