Chronic myeloid leukemia (CML), also called chronic myelogenous leukemia, is a blood cancer that starts in the bone marrow stem cells. A special change ...

Chronic myelogenous leukemia (CML) is a type of blood cancer that starts in the bone marrow, where blood cells are made. In CML, the bone marrow makes too many ...

Chronic myelocytic leukemia (CML) is a cancer of the blood and bone marrow, the soft part inside your bones that makes blood cells. In CML, a change (mutation) ...

Chronic granulocytic leukemia (CGL) is an older name for chronic myeloid leukemia (CML), a blood cancer that starts from the bone marrow cells that make white ...

BCR-ABL positive chronic myelogenous leukemia (CML) is a blood cancer that starts in the bone marrow, where new blood cells are made. In CML, a piece of ...

Chronic myelogenous leukemia, BCR-ABL1 positive (often called chronic myeloid leukemia or CML) is a blood cancer where the bone marrow makes too many white ...

Chronic multifocal osteomyelitis is a long-lasting inflammation of several bones that comes and goes over time. It usually happens in children and teenagers, ...

Chronic mucocutaneous candidiasis (CMC) is a rare immune system disorder where the body cannot properly fight Candida (yeast) infections on the skin, nails, ...

Chronic candidiasis of the mucosa, skin, and nails is a long-lasting or repeatedly returning yeast infection caused most often by Candida (especially Candida ...

Alpha-thalassemia–myelodysplastic syndrome (ATMDS)—also called acquired alpha-thalassemia with MDS, acquired HbH disease in MDS, or acquired α-thalassemia ...

Schindler disease type 3 is a very rare inherited condition. It happens when the body does not make enough of a lysosomal enzyme called ...

Alpha-N-acetylgalactosaminidase deficiency (often shortened to NAGA deficiency) is a very rare, inherited (passed from parents to children) condition. The body ...

Schindler disease type 2 is a very rare inherited (passed from parents) condition. It happens because the body does not make enough of an enzyme called ...

Kanzaki disease is a very rare inherited condition. It happens when the body does not have enough working of an enzyme called alpha-N-acetylgalactosaminidase ...

Adult-onset alpha-N-acetylgalactosaminidase deficiency is a very rare inherited (genetic) condition. In this condition, a body enzyme called ...

Alpha-N-acetylgalactosaminidase deficiency is a rare genetic condition in which the body does not make enough of an enzyme called ...

Alpha-N-acetylgalactosaminidase deficiency type 1 is a very rare, inherited (from both parents) disease of the body’s “recycling centers,” called lysosomes. In ...

Schindler disease is a very rare inherited (genetic) condition. People with this disorder do not have enough of an enzyme called ...

NAGA deficiency is a very rare inherited disease where the body does not make enough of an enzyme called alpha-N-acetylgalactosaminidase (often shortened to ...

Alpha-N-acetylgalactosaminidase—often shortened to alpha-NAGA—is a small worker-enzyme that lives inside the cell’s “recycling centers,” which are called ...