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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

Disease Browser
Parent Node: Leukemia, Lymphoid (D007945)
..Starting node ..Leukemia, T-Cell (D015458)
Child Nodes:
........Leukemia, Large Granular Lymphocytic (D054066)
........Leukemia, Prolymphocytic, T-Cell (D015461)
........Leukemia-Lymphoma, Adult T-Cell (D015459)
........N syndrome (C536108)
Sister Nodes:
..Leukemia, B-Cell (D015448) 2
..Leukemia, Biphenotypic, Acute (D015456)
..Leukemia, Prolymphocytic (D015463) 2
..Leukemia, T-Cell (D015458) 4
..Precursor Cell Lymphoblastic Leukemia-Lymphoma (D054198) 3
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6368
Name:	Leukemia, T-Cell
Definition:	A malignant disease of the T-LYMPHOCYTES in the bone marrow, thymus, and/or blood.
Alternative IDs:
ParentIDs:	MESH:D007945
TreeNumbers:	C04.557.337.428.580 \|C15.604.515.560.575 \|C20.683.515.528.582
Synonyms:	Leukemia, Lymphocytic, T Cell \|Leukemia, Lymphocytic, T-Cell \|Leukemias, T-Cell \|Leukemias, T-Cell Lymphocytic \|Leukemias, T Lymphocytic \|Leukemias, T-Lymphocytic \|Leukemia, T Cell \|Leukemia, T-Cell Lymphocytic \|Leukemia, T Lymphocytic \|Leukemia, T-Lymphocytic \|Ly
Slim Mappings:	Cancer\|Immune system disease\|Lymphatic disease
Reference:	MedGen: D015458 MeSH: D015458 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants