Nemaline myopathy 10 is a neuromuscular disorder caused by mutations in the LMOD3 gene that affects muscle structure and function. It is characterized...

Nemaline myopathy 2 is an inherited muscle disorder that primarily affects skeletal muscle function and strength. It arises from mutations in the NEB...

Nemaline myopathy 5, also known as Amish nemaline myopathy, is a subtype of nemaline myopathy that primarily affects skeletal muscles. It is caused by...

Nemaline myopathy 5B, autosomal recessive, childhood-onset is a congenital neuromuscular disorder that primarily affects skeletal muscle function. It...

Nemaline myopathy 6 is a muscle disorder affecting skeletal muscles that is caused by a mutation in the KBTBD13 gene, which plays an important role in...

Nemaline myopathy 7 is a form of congenital muscle disorder that is caused by mutations in the CFL2 gene. This condition primarily affects skeletal mu...

Nemaline myopathy 8 is an inherited muscle disorder that primarily affects skeletal muscles, leading to generalized muscle weakness. Caused by mutatio...

Nemaline myopathy 9 is a muscle disorder caused by pathogenic variants in the KLHL41 gene and is classified among the nemaline myopathies. It typicall...

Neonatal alloimmune neutropenia is a rare condition seen in newborns that is characterized by a low neutrophil count due to maternal antibodies target...

Neonatal anemia is a condition in which newborns exhibit lower than normal red blood cell counts. It is recognized as the mildest form of erythroblast...

Neonatal antiphospholipid syndrome, also known as neonatal Hughes syndrome or neonatal antiphospholipid antibody syndrome, is an extremely rare condit...

Neonatal autoimmune hemolytic anemia (neonatal AHA) is a rare condition characterized by the destruction of red blood cells in newborns, leading to an...

Neonatal dermatomyositis, also known as neonatal DM, is a very rare inflammatory condition that primarily presents in newborns with involvement of the...

Neonatal diabetes mellitus is a condition characterized by high blood sugar, failure to thrive, and in some cases, dehydration and severe ketoacidosis...

Neonatal diabetes mellitus with congenital hypothyroidism is a rare genetic disorder that affects multiple organ systems, most the endocrine system, g...

Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome is an ultra-rare, multi-system condition that presents in the neonatal period...