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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	January 28, 2025
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **4426 - 4450** of **5716** in total

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Disease ID	Disease Name	Gene Symbol	Gene ID ▲	Organism	Source
DOID:7596	asbestos-related lung carcinoma	RARB	5915	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050685	small cell carcinoma Aliases: Small cell carcinoma - intermediate cell Small cell carcinoma, intermediate cell intermediate cell small cell carcinoma	RB1 TERT	5925 7015	Homo sapiens (human)	Alliance of Genome Resources
DOID:4648	familial retinoblastoma Aliases: Hereditary Retinoblastoma	RB1	5925	Homo sapiens (human)	Alliance of Genome Resources
DOID:3407	carotid artery disease Aliases: disorder of carotid artery	Ltb4r	59264	Rattus norvegicus (Norway rat)	Alliance of Genome Resources
DOID:8552	chronic myeloid leukemia Aliases: CML CML - chronic Myelogenous Leukemia Myeloid Leukemia, chronic chronic granulocytic leukaemia chronic granulocytic leukemia chronic myelogenous leukaemia chronic myelogenous leukemia chronic myeloid leukaemia	Ncstn	59287	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0070013	Seckel syndrome 2 Aliases: SCKL2 Seckel-type dwarfism 2 microcephalic primordial dwarfism 2	RBBP8	5932	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110206	Charcot-Marie-Tooth disease dominant intermediate F Aliases: CMTDIF autosomal dominant intermediate Charcot-Marie-Tooth disease type F	GNB4	59345	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110393	retinitis pigmentosa 66 Aliases: RP66	RBP3	5949	Homo sapiens (human)	Alliance of Genome Resources
DOID:13910	red color blindness Aliases: Protan defect Protanopia	OPN1LW	5956	Homo sapiens (human)	Alliance of Genome Resources
DOID:11105	fundus albipunctatus Aliases: Pigmentary retinal dystrophy retinitis punctata albescens	PRPH2 RDH5 RHO RLBP1	5959 5961 6010 6017	Homo sapiens (human)	Alliance of Genome Resources
DOID:8499	night blindness Aliases: nyctalopia	GRK1 NYX RDH5 RHO RLBP1	5959 6010 6011 6017 60506	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110383	retinitis pigmentosa 7 Aliases: RP7	PRPH2 ROM1	5961 6094	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060863	patterned macular dystrophy Aliases: patterned dystrophy of retinal pigment epithelium	PRPH2	5961	Homo sapiens (human)	Alliance of Genome Resources
DOID:0060866	patterned macular dystrophy 1 Aliases: MDPT1 butterfly-shaped pigmentary maculary dystrophy 1	PRPH2	5961	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110482	autosomal recessive nonsyndromic deafness 24 Aliases: DFNB24 autosomal recessive deafness 24	RDX	5962	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111992	immunodeficiency 53 Aliases: IMD53	RELB	5971	Homo sapiens (human)	Alliance of Genome Resources
DOID:10881	hand, foot and mouth disease Aliases: HFMD Vesicular stomatitis and exanthem	REN	5972	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080280	gingival fibromatosis 5	REST	5978	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110556	autosomal dominant nonsyndromic deafness 27 Aliases: DFNA27 autosomal dominant deafness 27	REST	5978	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080204	renal hypoplasia	RET	5979	Homo sapiens (human)	Alliance of Genome Resources
DOID:10016	multiple endocrine neoplasia type 2B Aliases: MEN type IIB MEN2B Multiple endocrine neoplasia, type 3 Wagenmann-Froboese syndrome mucosal neuroma syndrome	RET	5979	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050430	multiple endocrine neoplasia type 2A Aliases: MEN2A Sipple syndrome multiple endocrine neoplasia II	RET	5979	Homo sapiens (human)	Alliance of Genome Resources
DOID:0050547	familial medullary thyroid carcinoma Aliases: THYROID CARCINOMA, FAMILIAL MEDULLARY	RET	5979	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110394	retinitis pigmentosa 44 Aliases: RP44	RGR	5995	Homo sapiens (human)	Alliance of Genome Resources
DOID:0081112	Baraitser-Winter syndrome 1	ACTB	60	Homo sapiens (human)	Alliance of Genome Resources

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