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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 **8126 - 8150** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:0080465	developmental and epileptic encephalopathy 30 Aliases: DEE30 early infantile epileptic encephalopathy 30	KIN1 KIN2	850785 851700	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0060668	anencephaly	KIN1 KIN2	850785 851700	Saccharomyces cerevisiae S288C	Alliance of Genome Resources
DOID:0080827	human cytomegalovirus infection	KIR3DS1 REN	3813 5972	Homo sapiens (human)	Alliance of Genome Resources
DOID:0040086	Polyomavirus-associated nephropathy Aliases: PVAN polyomavirus associated nephropathy	KIR3DS1	3813	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112266	nephrotic syndrome type 23 Aliases: NPHS23	KIRREL1	55243	Homo sapiens (human)	Alliance of Genome Resources
DOID:3113	papillary carcinoma	KISS1R VEGFC	7424 84634	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112310	central precocious puberty 1 Aliases: CPPB1	KISS1R	84634	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090074	hypogonadotropic hypogonadism 8 with or without anosmia	KISS1R	84634	Homo sapiens (human)	Alliance of Genome Resources
DOID:8440	ileus Aliases: Ileus of intestine	KIT MMP9 NOS3	3815 4318 4846	Homo sapiens (human)	Alliance of Genome Resources
DOID:5389	oxyphilic adenoma Aliases: Follicular adenoma, oxyphilic cell Oncocytoma	KIT	3815	Homo sapiens (human)	Alliance of Genome Resources
DOID:2361	macrocytic anemia Aliases: ANEMIA MACROCYTIC Macrocytic anaemia	KIT	3815	Homo sapiens (human)	Alliance of Genome Resources
DOID:962	neurofibroma	KIT	3815	Homo sapiens (human)	Alliance of Genome Resources
DOID:4226	endometrial stromal sarcoma Aliases: ESS Undifferentiated endometrial sarcoma endometrial stromal sarcoma, high grade	KIT	3815	Homo sapiens (human)	Alliance of Genome Resources
DOID:6171	uterine carcinosarcoma Aliases: mixed mullerian sarcoma of uterus	KIT	3815	Homo sapiens (human)	Alliance of Genome Resources
DOID:3263	piebaldism Aliases: PIEBALD TRAIT Partial albinism	KIT	3815	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110590	autosomal dominant nonsyndromic deafness 69 Aliases: DCUA DFNA69 autosomal dominant deafness 69 unilateral or asymmetric congenital deafness	KITLG	4254	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111373	familial progressive hyperpigmentation with or without hypopigmentation Aliases: FPHH MUH melanosis universalis hereditaria	KITLG	4254	Homo sapiens (human)	Alliance of Genome Resources
DOID:2247	spondylosis Aliases: Lumbar spondylosis with myelopathy Spondylogenic compression of lumbar spinal cord Spondylogenic compression of thoracic spinal cord Thoracic or lumbar spondylosis with myelopathy lumbosacral spondylosis without myelopathy spondylosis with myelopathy	KL	9365	Homo sapiens (human)	Alliance of Genome Resources
DOID:4372	intracranial embolism Aliases: Cerebral embolism with cerebral infarction cerebral embolism	KL	9365	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060491	SPOAN syndrome Aliases: spastic paraplegia, optic atropy, and neuropathy spastic paraplegia, optic atropy, and neuropathy syndrome	KLC2	64837	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110386	retinitis pigmentosa 42 Aliases: RP42	KLHL7	55975	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080331	cold-induced sweating syndrome 3	KLHL7	55975	Homo sapiens (human)	Alliance of Genome Resources
DOID:363	uterine cancer Aliases: CA - cancer of uterus Tumour of uterus malignant neoplasm of uterus malignant uterine tumor neoplasm of uterus uterine tumor uterus neoplasm	KLK10 L1CAM	3897 5655	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110057	amelogenesis imperfecta type 2A1 Aliases: AI2A1 amelogenesis imperfecta pigmented hypomaturation type 1 amelogenesis imperfecta type IIA1	KLK4	9622	Homo sapiens (human)	Alliance of Genome Resources
DOID:4231	histiocytoma	KLRC4-KLRK1 KLRK1	100528032 22914	Homo sapiens (human)	Alliance of Genome Resources

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