Monogenic diabetes is a form of diabetes mellitus caused by a mutation in a single gene, which leads to abnormal blood sugar regulation. Recognized su...

Monogenic epilepsy is a neurologic condition primarily characterized by recurrent seizures and associated developmental challenges. It is a geneticall...

Monomelic amyotrophy is a benign lower motor neuron disorder that primarily affects the distal upper extremities during adolescence. The condition is...

Mononen-Karnes-Senac syndrome is a rare condition that affects the skeleton. This syndrome is mainly characterized by abnormalities in the hands and f...

Mononeuritis multiplex is a painful, asymmetric peripheral neuropathy that involves damage to at least two separate nerve areas, leading to both senso...

Mononeuritis simplex is a condition characterized by the inflammation of a single nerve. It is defined by localized nerve involvement, which can lead...

Mononeuropathy is a condition that involves injury or dysfunction of a single peripheral nerve, and in some cases, multiple isolated nerve injuries ma...

Monophasic synovial sarcoma is a type of soft tissue malignancy that is characterized by the presence of either an epithelial or a spindle cell compon...

Monosomy is a chromosomal abnormality characterized by the absence of one chromosome from the normal diploid set. This condition affects multiple syst...

Monosomy 21 is a chromosomal anomaly characterized by the loss of variable portions of the long arm of chromosome 21, which can lead to an increased r...

Monosomy 22 is a chromosomal condition characterized by the loss of genetic material normally present on chromosome 22. This disorder affects multiple...

Monosomy 7 myelodysplasia and leukemia syndrome 1 is a condition that primarily affects the blood and bone marrow, predisposing individuals to the dev...

Monosomy 7 myelodysplasia and leukemia syndrome 2 is an inherited condition linked to alterations in the SAMD9 gene. It is associated with disruptions...

Monosomy 9q22.3, also known as microdeletion 9q22.3, is a chromosomal deletion disorder that affects growth and neurodevelopment. Affected individuals...

Monosomy chromosome 8 is a chromosomal disorder characterized by the complete absence of one copy of chromosome 8. This condition is defined by a chro...

Monosomy X is a chromosomal condition that results from the absence of all or part of one of the sex chromosomes, primarily affecting individuals who...

Monostotic fibrous dysplasia is a skeletal condition in which normal bone is gradually replaced by fibrous tissue in a single bone, leading to potenti...