MMD
Description
The MMD (monocyte to macrophage differentiation associated) is a protein-coding gene located on chromosome 17.
MMD may refer to:
MMD plays a role in regulating the movement and activity of lysosomal membranes, particularly during the activation of microglia (immune cells in the brain) after a brain injury.
MMD is also known as MMA, MMD1, PAQR11.
Associated Diseases
- immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias
- hyper-IgM syndrome type 3
- autoimmune lymphoproliferative syndrome
- glycoprotein storage disease
- immunodeficiency 105
- immunodeficiency 75
- osteoarthritis
- autoimmune lymphoproliferative syndrome type 2A
- hyper-IgM syndrome type 5
- X-linked retinoschisis
- X-linked retinal dysplasia
- immunodeficiency 78 with autoimmunity and developmental delay
- immunodeficiency 72 with autoinflammation
- immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia
