GlyCosmos Portal

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

Displaying entries **6601 - 6625** of **7942** in total

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Disease ID	Disease Name	Gene Symbol ▼	Gene ID	Organism
DOID:0111132	focal segmental glomerulosclerosis 7 Aliases: FSGS7	ACE	1636	Homo sapiens (human)
DOID:0060610	megacystis-microcolon-intestinal hypoperistalsis syndrome Aliases: Berdon syndrome Megacystis microcolon intestinal hypoperistalsis syndrome megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH visceral myopathy	ACE	1636	Homo sapiens (human)
DOID:0111425	restrictive cardiomyopathy 1 Aliases: RCM1 familial restrictive cardiomyopathy 1	ACE	1636	Homo sapiens (human)
DOID:0111130	focal segmental glomerulosclerosis 5 Aliases: FSGS5	ACE	1636	Homo sapiens (human)
DOID:0111129	focal segmental glomerulosclerosis 2 Aliases: FSGS2	ACE	1636	Homo sapiens (human)
DOID:0111131	focal segmental glomerulosclerosis 6 Aliases: FSGS6	ACE	1636	Homo sapiens (human)
DOID:13452	scleritis	ACE TNF	1636 7124	Homo sapiens (human)
DOID:12185	otosclerosis	ACE SLC26A2	1636 1836	Homo sapiens (human)
DOID:0060071	pre-malignant neoplasm	ACE SFTPD TP53	1636 6441 7157	Homo sapiens (human)
DOID:5511	dysgerminoma of ovary Aliases: Ovarian Dysgerminoma	ACE PTEN	1636 5728	Homo sapiens (human)
DOID:790	ocular hypotension Aliases: Hypotony of eye	ACE PRNP	1636 5621	Homo sapiens (human)
DOID:0050851	glomerulosclerosis	ACE PLA2G7	1636 7941	Homo sapiens (human)
DOID:3500	gallbladder adenocarcinoma Aliases: adenocarcinoma of the gallbladder	ACE NT5E OGG1 SOAT1	1636 4907 4968 6646	Homo sapiens (human)
DOID:0111112	nephronophthisis 1 Aliases: NPH1 NPHP1 juvenile nephronophthisis 1	ACE MLYCD STS UMOD	1636 23417 412 7369	Homo sapiens (human)
DOID:12574	posterior uveitis Aliases: Uveitis, posterior	ACE ICAM1	1636 3383	Homo sapiens (human)
DOID:8886	chorioretinitis Aliases: retinochoroiditis	ACE ICAM1	1636 3383	Homo sapiens (human)
DOID:11406	choroiditis	ACE ICAM1	1636 3383	Homo sapiens (human)
DOID:559	acute pyelonephritis	ACE ICAM1 MBL2 PTGS2 RBP4 SMUG1 UGT1A1	1636 23583 3383 4153 54658 5743 5950	Homo sapiens (human)
DOID:0050474	Netherton syndrome	ACE GBA1 ICAM1 PTGS2	1636 2629 3383 5743	Homo sapiens (human)
DOID:593	agoraphobia Aliases: Fear of open spaces	ACE GAD1	1636 2571	Homo sapiens (human)
DOID:3341	osteitis fibrosa Aliases: Osteitis fibrosa cystica generalisata Von Recklinghausen's bone disease hyperparathyroid bone disease	ACE G6PD KL OCRL PLCB3 PTGS2 SDHB SMUG1	1636 23583 2539 4952 5331 5743 6390 9365	Homo sapiens (human)
DOID:13543	hyperparathyroidism	ACE G6PD KL OCRL PLCB3 PTGS2 SDHB SMUG1	1636 23583 2539 4952 5331 5743 6390 9365	Homo sapiens (human)
DOID:1591	renovascular hypertension	ACE FIG4 G6PD PKD1 PTGS1 PTGS2 SLC33A1 TM7SF2	1636 2539 5310 5742 5743 7108 9197 9896	Homo sapiens (human)
DOID:397	restrictive cardiomyopathy Aliases: Cardiomyopathy, constrictive primary restrictive cardiomyopathy	ACE ENPP1 PIGT SCD5 SCD XYLT1 XYLT2	1636 51604 5167 6319 64131 64132 79966	Homo sapiens (human)
DOID:12157	aseptic meningitis Aliases: acute aseptic meningitis	ACE ENO2 ICAM1 MRC1 TPI1	1636 2026 3383 4360 7167	Homo sapiens (human)

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