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GlyCosmos Diseases

List of diseases involving glycan related genes. The information of each database of Glyco-Disease Genes Database (GDGDB), DisGeNET, and Alliance of Genome Resources is integrated into one list.

Source	Last Updated
Alliance of Genome Resources	July 29, 2024
DisGeNET	July 29, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **1276 - 1300** of **4621** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism
DOID:2024	placental choriocarcinoma Aliases: Choriocarcinoma of the Placenta	CYP19A1 STS	1588 412	Homo sapiens (human)
DOID:14039	POEMS syndrome	CYP19A1 SDC1	1588 6382	Homo sapiens (human)
DOID:9042	polyp of corpus uteri Aliases: endometrial/uterine polyp polyp of Endometrium polyp of the Uterus polyp, uterus	CYP19A1 PTEN PTGS2 SDC1	1588 5728 5743 6382	Homo sapiens (human)
DOID:3781	anovulation	CYP19A1 PAPSS2	1588 9060	Homo sapiens (human)
DOID:12559	idiopathic juvenile osteoporosis Aliases: Idiopathic osteoporosis juvenile osteoporosis	CYP19A1 LRP5	1588 4041	Homo sapiens (human)
DOID:2696	Leydig cell tumor Aliases: Leydig cell neoplasm	CYP19A1 LCT LGALS3 PTGES PTGS2 SMUG1	1588 23583 3938 3958 5743 9536	Homo sapiens (human)
DOID:1100	ovarian disease	CYP19A1 KLB	152831 1588	Homo sapiens (human)
DOID:12577	urethral obstruction Aliases: Obstruction of urethra	CYP19A1 HPSE2 SIRT2	1588 22933 60495	Homo sapiens (human)
DOID:4226	endometrial stromal sarcoma Aliases: ESS Undifferentiated endometrial sarcoma endometrial stromal sarcoma, high grade	CYP19A1 HPRT1 NCAM1 TKTL1	1588 3251 4684 8277	Homo sapiens (human)
DOID:14654	prostatitis	CYP19A1 HADHA HADHB PTGS2 SMUG1	1588 23583 3030 3032 5743	Homo sapiens (human)
DOID:4926	bronchiolo-alveolar adenocarcinoma Aliases: Bronchioalveolar lung carcinoma Bronchioloalveolar carcinoma Minimally Invasive Lung Adenocarcinoma	CYP19A1 GPX3 GPX7 HPGDS HSD11B1 HYAL2 MDH2 NCAM1 PIK3CA PTEN SFTPA2 SFTPC SLC2A10 TP53	1588 27306 2878 2882 3290 4191 4684 5290 5728 6440 7157 729238 81031 8692	Homo sapiens (human)
DOID:1921	Klinefelter syndrome Aliases: 47, XXY Hypogonadotropic Hypogonadism Klinefelter's syndrome XXY syndrome XXY trisomy	CYP19A1 EBP GK IL1RAPL1 PNPLA6 SOAT1 STS	10682 10908 11141 1588 2710 412 6646	Homo sapiens (human)
DOID:0060243	stuttering Aliases: familial persistent stuttering stammering	CYP19A1 DLD DPAGT1 GNPTAB GNPTG INPP5D NAGPA PTGDS	1588 1738 1798 3635 51172 5730 79158 84572	Homo sapiens (human)
DOID:13948	bladder neck obstruction Aliases: Obstruction of bladder neck or vesicourethral orifice	CYP19A1 DCN HTR2A PTEN PTGS2	1588 1634 3356 5728 5743	Homo sapiens (human)
DOID:0080369	ovarian sex-cord stromal tumor	CYP19A1 CYP2B6	1555 1588	Homo sapiens (human)
DOID:192	sex cord-gonadal stromal tumor Aliases: Sex Cord-Stromal neoplasm Sex cord stromal tumour Specialized gonadal neoplasm Specialized gonadal tumor Specialized gonadal tumour sex cord-gonadal stromal tumour	CYP19A1 CYP2B6 LGALS3	1555 1588 3958	Homo sapiens (human)
DOID:2691	myoma Aliases: benign neoplasm of the Muscle	CYP19A1 CYP2B6 HPSE	10855 1555 1588	Homo sapiens (human)
DOID:229	female reproductive system disease	CYP19A1 CYP1A1 CYP1A2 CYP2B6 LGALS9	1543 1544 1555 1588 3965	Homo sapiens (human)
DOID:3306	mixed germ cell cancer Aliases: mixed germ cell neoplasm mixed germ cell tumor mixed germ cell tumour mixed teratoma and seminoma	CYP17A1	1586	Homo sapiens (human)
DOID:6676	Froelich syndrome Aliases: Babinski-Froelich syndrome Froehlich syndrome Froehlich's syndrome Froelich's syndrome adiposogenital syndrome	CYP17A1	1586	Homo sapiens (human)
DOID:13868	hypoactive sexual desire disorder Aliases: Lack or loss of sexual desire	CYP17A1	1586	Homo sapiens (human)
DOID:0111341	primary failure of tooth eruption Aliases: PFE dental noneruption familial posterior openbite malocclusion nonsyndromic primary failure of eruption primary retention of teeth unerupted second primary molar	CYP17A1	1586	Homo sapiens (human)
DOID:0080479	peroxisome biogenesis disorder 4A Aliases: peroxisome biogenesis disorder 4A (Zellweger)	CYP17A1	1586	Homo sapiens (human)
DOID:0090088	hypogonadotropic hypogonadism 24 without anosmia Aliases: isolated follicle-stimulating hormone deficiency	CYP17A1 CYP19A1	1586 1588	Homo sapiens (human)
DOID:5119	ovarian cyst	CYP17A1 CYP19A1 NTHL1 PIK3CA PTEN PTGS1 PTGS2	1586 1588 4913 5290 5728 5742 5743	Homo sapiens (human)

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