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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 (D007938)
Parent Node: Lymphoproliferative Disorders (D008232)
..Starting node ..Leukemia, Lymphoid (D007945)
Child 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
Sister Nodes:
..Agammaglobulinemia (D000361) 19
..Autoimmune Lymphoproliferative Syndrome (D056735) 5
..Giant Lymph Node Hyperplasia (D005871) 2
..Granuloma (D006099) 17
..Heavy Chain Disease (D006362) 7
..Immunoblastic Lymphadenopathy (D007119)
..Immunoproliferative Small Intestinal Disease (D007161)
..Infectious Mononucleosis (D007244)
..Leukemia, Hairy Cell (D007943)
..Leukemia, Lymphoid (D007945) 14
..Lymphangiomyoma (D008203) 1
..Lymphoma (D008223) 36
..Lymphoproliferative Syndrome, Ebv-Associated, Autosomal, 1 (C567815)
..Lymphoproliferative Syndrome, X-Linked, 2 (C564469)
..Macrophage Activation Syndrome (D055501)
..Marek Disease (D008380)
..Multiple Myeloma (D009101) 1
..Plasmacytoma (D010954) 1
..Sarcoidosis (D012507) 4
..Sezary Syndrome (D012751)
..Tumor Lysis Syndrome (D015275)
..Waldenstrom Macroglobulinemia (D008258)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6345
Name:	Leukemia, Lymphoid
Definition:	Leukemia associated with HYPERPLASIA of the lymphoid tissues and increased numbers of circulating malignant LYMPHOCYTES and lymphoblasts.
Alternative IDs:
ParentIDs:	MESH:D007938\|MESH:D008232
TreeNumbers:	C04.557.337.428 \|C15.604.515.560 \|C20.683.515.528
Synonyms:	Leukemia, Lymphocytic \|Leukemias, Lymphocytic \|Leukemias, Lymphoid \|Lymphocytic Leukemia \|Lymphocytic Leukemias \|Lymphoid Leukemia \|Lymphoid Leukemias
Slim Mappings:	Cancer\|Immune system disease\|Lymphatic disease
Reference:	MedGen: D007945 MeSH: D007945 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants