Disease Directory

B-lymphoblastic leukemia/lymphoma MLL rearranged is a type of cancer that affects blood cells. This condition is defined by the presence of abnormal l...

B-lymphoblastic leukemia/lymphoma with ETV6-RUNX1 is a type of blood cancer where immature white blood cells, known as lymphoblasts, are present. In t...

B-lymphoblastic leukemia/lymphoma with IAMP21 is a type of blood cancer that affects B-lymphoblast cells. It is defined by the abnormal amplification...

B-lymphoblastic leukemia/lymphoma with IL3-IGH is a rare type of blood cancer that involves B-lymphoblasts. These are immature cells that normally gro...

Information about overview is currently limited for this condition.

B-lymphoblastic leukemia/lymphoma with hypodiploidy, also known as Hypodiploid ALL, is a rare type of cancer that affects immature B lymphocytes. In t...

B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality is a rare type of blood cancer that affects B-lymphoblasts, which are immature wh...

Information about the overview of this condition is currently limited for this condition.

Information about the overview is currently limited for this condition. B-lymphoblastic leukemia/lymphoma with t(17;19) is a rare disorder, and detail...

B-lymphoblastic leukemia/lymphoma with t(5;14)(q31.1;q32.3) is a rare form of blood cancer that affects B-cell precursors. This condition is noted by...

Detailed information about this condition is currently limited. B-lymphoblastic leukemia/lymphoma with t(7;9)(q11.2;p13.2) is a rare blood cancer that...

Information about the overview is currently limited for this condition.

B-lymphoblastic leukemia/lymphoma with t(v;11q23.3) is a rare type of blood cancer that affects immature B cells. It is known by several names, includ...

B-lymphoblastic leukemia/lymphoma, BCR-ABL1–like is a type of blood cancer that affects B-lymphoblasts, which are immature cells in the blood. This co...

B3GALT6-congenital disorder of glycosylation is a rare inherited condition that occurs because of a mutation in the B3GALT6 gene. This mutation affect...

B4GALT1-congenital disorder of glycosylation (B4GALT1-CDG) is a very rare genetic condition that affects the process of glycosylation, where sugars ar...

BAP1-related tumor predisposition syndrome is an inherited condition that increases the risk of developing several types of cancer. It is linked to ha...

BARD1-related cancer predisposition is a hereditary condition caused by variations in the BARD1 gene. These gene changes increase the risk of developi...

BBS1-related ciliopathy is a type of condition caused by changes (variants) in the BBS1 gene. It belongs to a broader group of disorders known as cili...

BBS10-related ciliopathy is a condition caused by changes (variants) in the BBS10 gene. This gene plays a role in the function of cilia, which are sma...