Directory
Miller syndrome
Miller syndrome is a rare genetic disorder characterized by a combination of various abnormalities, including skeletal developmental disorders,...
Miller-Dieker syndrome
Miller-Dieker syndrome (MDS) is a rare genetic disorder caused by the loss of a region of the ...
Miller Fisher syndrome
Miller Fisher syndrome (MFS) is a rare but significant variant of Guillain-Barré syndrome that is characterized by an acute infectious ...
Mohr-Tranebjerg syndrome
Mohr-Tranebjerg syndrome (MTS) is a rare inherited disorder that manifests itself as a combination of multiple neurological...
Morgagni-Stewart-Morel syndrome
Morgagni-Stewart-Morel syndrome (Morel, 1896) is a rare hereditary disorder characterized by facial anomalies...
Mounier-Kuhn syndrome
Mounier-Kuhn syndrome (spinal muscular atrophy type 2) is a rare genetic disorder characterized by progressive ...
Muir-Torre syndrome
Muir-Torre syndrome (MTS) is a rare genetic disorder that combines features of the inherited syndrome...
May-Turner syndrome
May-Thurner syndrome (or Turner syndrome) is a genetic disorder associated with abnormalities in the development and function of the reproductive organs.
Mallory-Weiss syndrome
Mallory-Weiss syndrome is an anomaly characterized by tears in the lining of the esophagus at the junction with the stomach...
Münke's syndrome
Muenke syndrome is an autosomal dominant disorder belonging to the group of craniosynostoses characterized by...
Munchausen syndrome by proxy
Munchausen syndrome by proxy (MSBPP) is a complex and often perplexing psychopathological condition in which a person...
Mast Cell Activation Syndrome (MCAS)
Mast cell activation syndrome (MCAS) is a clinical syndrome characterized by a systemic response to a variety of tr...
Meconium aspiration syndrome
Meconium aspiration syndrome (MAS) is a severe condition in newborns that results from the aspiration of meconium, the primary...
Megalencephaly-capillary malformation syndrome
Megalencephaly-capillary malformation syndrome (MCM) is a rare disorder characterized by enlargement of the brain...
Microphthalmos syndrome 9
Microphthalmos syndrome (microphthalmos) is a birth defect characterized by abnormally small size of one or both eyes...
Microphthalmia syndrome with linear skin defects
Microphthalmia with linear skin defects (MCDK) syndrome is a rare genetic disorder characterized by the development of...
Microcephaly and deafness syndrome
Microcephaly and deafness syndrome is a complex of neurological and sensory impairments characterized by a decrease in the size of the...
X-linked multiple pterygoid syndrome
X-linked multiple pterygoid syndrome (X-linked lichen multiplex syndrome) is a rare genetic disorder that causes...
Multiple pterygoid hymen syndrome
Multiple pterygoid syndrome (MPS) is a rare genetic disorder caused by abnormalities in the development of the...
Multiple synostosis syndrome 1
Multiple synostosis syndrome (MSS) is a rare genetic disorder characterized by abnormal fusion of the bones of the skull and other...
Mosaic variegated aneuploidy syndrome
Mosaic variegated aneuploidy syndrome (MVAS) is a genetic disorder characterized by chromosomal abnormalities where...
Multicentric carpotarsal osteolysis syndrome
Multicentric carpotarsal osteolysis (MCTO) syndrome is a rare disorder characterized by progressive...
McLeod neuroacanthocytosis syndrome
McLeod neuroacanthocytosis syndrome is a rare inherited neurological disorder characterized by specific changes in the...
Median arcuate ligament syndrome (MALS)
Median arcuate ligament syndrome (MALS) is a clinical condition resulting from compression of the abdominal...
Mixed gonadal dysgenesis
Mixed gonadal dysgenesis (MGD) is a rare genetic disorder characterized by abnormal development of the gonads that...
Mixed connective tissue disease
Mixed connective tissue disease (MCTD) is a clinical syndrome that includes elements of several connective tissue diseas...
Stenosis of the external opening of the urethra
Stenosis of the external urethral opening (SUE) is a narrowing of the urethra in the area of the external...
MYH9-associated thrombocytopenia
MYH9-associated thrombocytopenia is an inherited disorder characterized by low levels of platelets in the blood...
Morning sickness
Morning sickness is a symptom that is most common during pregnancy, but can also be a manifestation of various...
Myocardial contusion
Myocardial contusion, or heart muscle injury, is damage to the heart tissue caused by mechanical action that may...
