GlyCosmos Portal

Source	Last Updated
Alliance of Genome Resources	October 9, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017

Displaying entries **7151 - 7175** of **15957** in total

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Disease ID	Disease Name	Gene Symbol ▲	Gene ID	Organism	Source
DOID:525	central nervous system vasculitis	H2-D1 H2-K1 H2-Q10 H2-Q1 H2-Q2 H2-Q4 H2-Q6 H2-Q7	110557 14964 14972 15006 15007 15013 15015 15018	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1761	Melkersson-Rosenthal syndrome Aliases: Cheilitis granulomatosa of Mescher-Melkersson-Rosenthal Melkersson's syndrome	H2-D1 H2-K1 H2-Q10 H2-Q1 H2-Q2 H2-Q4 H2-Q6 H2-Q7	110557 14964 14972 15006 15007 15013 15015 15018	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1024	leprosy	H2-Eb1 Il17a Lta Slc11a1 Tlr1 Tlr2 Tnf	14969 16171 16992 18173 21897 21926 24088	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:13404	uveoparotid fever Aliases: Heerfordt's syndrome	H2-Eb1	14969	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:12029	sympathetic ophthalmia Aliases: Sympathetic uveitis	H2-Eb1	14969	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:1395	schistosomiasis	H2-Eb1	14969	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0080684	diffuse midline glioma, H3 K27M-mutant Aliases: diffuse intrinsic pontine glioma	H3-3A H3-3B	3020 3021	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090139	cortisone reductase deficiency Aliases: CORTRD	H6PD HSD11B1	3290 9563	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090141	cortisone reductase deficiency 1 Aliases: CORTRD1	H6PD	9563	Homo sapiens (human)	Alliance of Genome Resources
DOID:0090139	cortisone reductase deficiency Aliases: CORTRD	H6pd Hsd11b1	100198 15483	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0090141	cortisone reductase deficiency 1 Aliases: CORTRD1	H6pd	100198	Mus musculus (house mouse)	Alliance of Genome Resources
DOID:0081337	congenital myopathy	HACD1 LDB3 MYBPC1	11155 4604 9200	Homo sapiens (human)	Alliance of Genome Resources
DOID:0070215	familial hyperinsulinemic hypoglycemia 4 Aliases: HHF4 hyperinsulinemic hypoglycemia due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency hyperinsulinism due to SCHAD deficiency hyperinsulinism due to glutamodehydrogenase deficiency hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency	HADH	3033	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111277	mitochondrial trifunctional protein deficiency Aliases: MTPD TFP deficiency TFPD	HADHA HADHB	3030 3032	Homo sapiens (human)	Alliance of Genome Resources
DOID:700	mitochondrial metabolism disease	HADHB IARS2 LARS2 LETM2 MARS2 NDUFS1 SLC25A6 UQCRFS1 VARS1 WARS2 YME1L1	10352 10730 137994 23395 293 3032 4719 55699 7386 7407 92935	Homo sapiens (human)	Alliance of Genome Resources
DOID:0112133	severe congenital neutropenia 3 Aliases: Kostmann disease Kostmann syndrome SCN3 infantile agranulocytosis	HAX1	10456	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111363	Heinz body anemia	HBA1 HBA2 HBB	3039 3040 3043	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111631	familial erythrocytosis 7 Aliases: ECYT7 alpha-globin type erythrocytosis alpha-globin type polycythemia	HBA1 HBA2	3039 3040	Homo sapiens (human)	Alliance of Genome Resources
DOID:0110031	hemoglobin H disease Aliases: HBH alpha thalassemia, haemoglobin H type alpha thalassemia, hemoglobin H type alpha-thalassemia intermedia haemoglobin H disease haemoglobin H disease, deletional hemoglobin H disease, deletional	HBA1 HBA2	3039 3040	Homo sapiens (human)	Alliance of Genome Resources
DOID:1584	acute chest syndrome Aliases: acute chest syndrome in sickle cell disease	HBB NOS3 VEGFA	3043 4846 7422	Homo sapiens (human)	Alliance of Genome Resources
DOID:2860	hemoglobinopathy Aliases: hemoglobinopathies	HBB	3043	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080770	autosomal dominant beta thalassemia Aliases: inclusion body beta-thalassemia	HBB	3043	Homo sapiens (human)	Alliance of Genome Resources
DOID:0080773	delta beta-thalassemia	HBB	3043	Homo sapiens (human)	Alliance of Genome Resources
DOID:2859	hemoglobin C disease Aliases: Hb-C disease	HBB	3043	Homo sapiens (human)	Alliance of Genome Resources
DOID:0111632	familial erythrocytosis 6 Aliases: ECYT6 beta-globin type erythrocytosis beta-globin type polycythemia	HBB	3043	Homo sapiens (human)	Alliance of Genome Resources

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