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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes

Disease Browser
Parent Node: Anemia (D000740)
..Starting node ..Anemia, Hemolytic (D000743)
Child Nodes:
........6-Phosphogluconolactonase Deficiency (C566803)
........Adenosine Deaminase, Elevated, Hemolytic Anemia Due To (C566314)
........Adenylate Kinase Deficiency, Hemolytic Anemia Due To (C567228)
........Anemia, Hemolytic, Autoimmune (D000744) 6
........Anemia, Hemolytic, Congenital (D000745) 68
........CD59 Deficiency (C567355)
........Favism (D005236)
........Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to (C565557)
........Glutathione Peroxidase Deficiency, Hemolytic Anemia possibly due to (C564217)
........Glutathione Reductase, Hemolytic Anemia due to Deficiency of, in Red Cells (C564218)
........Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to (C565545)
........Heme Oxygenase 1 Deficiency (C564200)
........Hemoglobinuria, Paroxysmal (D006457) 2
........Hemolytic Anemia with Thermal Sensitivity of Red Cells (C565522)
........HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY (OMIM:235700)
........Hemolytic Poikilocytic Anemia due to Reduced Ankyrin Binding Sites (C564197)
........Hemolytic-Uremic Syndrome (D006463) 2
........Hexokinase Deficiency Hemolytic Anemia (C562995)
........Paroxysmal Exertion-Induced Dyskinesia And Hemolytic Anemia (C567412)
........Renal Tubular Acidosis, Distal, With Hemolytic Anemia (C566910)
........SYSTEMIC LUPUS ERYTHEMATOSUS WITH HEMOLYTIC ANEMIA, SUSCEPTIBILITY TO, 1 (OMIM:607279)
Sister Nodes:
..Anemia, Aplastic (D000741) 31
..Anemia, Hemolytic (D000743) 98
..Anemia, Hypochromic (D000747) 3
..Anemia, Macrocytic (D000748) 10
..Anemia, Myelophthisic (D000750)
..Anemia, Neonatal (D000751) 2
..Anemia, Refractory (D000753) 2
..Anemia, Sideroblastic (D000756) 8
..Anemia, X-Linked, without Thrombocytopenia (C564429)
..Dyserythropoiesis, Congenital, with Internuclear Chromatin Bridges and Ultrastructurally Normal Erythroblast Heterochromatin (C566368)
..Hyperuricemic Nephropathy, Familial Juvenile 2 (C567760)
..Red-Cell Aplasia, Pure (D012010) 13
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	627
Name:	Anemia, Hemolytic
Definition:	A condition of inadequate circulating red blood cells (ANEMIA) or insufficient HEMOGLOBIN due to premature destruction of red blood cells (ERYTHROCYTES).
Alternative IDs:
ParentIDs:	MESH:D000740
TreeNumbers:	C15.378.071.141
Synonyms:	Acquired Hemolytic Anemia \|Anemia, Acquired Hemolytic \|Anemia, Hemolytic, Acquired \|Anemia, Microangiopathic \|Hemolytic Anemia \|Hemolytic Anemia, Acquired \|Microangiopathic Anemia \|Microangiopathic Hemolytic Anemia
Slim Mappings:	Blood disease
Reference:	MedGen: D000743 MeSH: D000743 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants