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Disease	Synonyms	Description	Articles
mixed cerebral palsy		A cerebral palsy that is caused by injury to both ..[+] A cerebral palsy that is caused by injury to both the pyramidal and extra pyramidal areas of the brain, which results in both the tight muscle tone and the involuntary movements. The individual have difficulty with speaking and swallowing. [-]
malignant pleural solitary fibrous tumor		n_a
methylmalonic aciduria and homocystinuria type cblC	MAHCC; Cobalamin C deficiency	A methylmalonic acidemia that has_material_basis_i..[+] A methylmalonic acidemia that has_material_basis_in deficiency in synthesis of both AdoCbl and MeCbl (cblC) and is characterized by decreased levels of the coenzymes adenosylcobalamin (AdoCbl) and methylcobalamin (MeCbl), which results in decreased activity of the respective enzymes methylmalonyl-CoA mutase. [-]
methylmalonic aciduria and homocystinuria type cblD	MAHCD; Cobalamin D deficiency	A methylmalonic aciduria that is characterized by ..[+] A methylmalonic aciduria that is characterized by combined homocystinuria and methylmalonic aciduria and deficiency of MCM and MS activities. [-]
methylmalonic aciduria and homocystinuria type cblF	MAHCF; Cobalamin F deficiency	A methylmalonic acidemia that is characterized by ..[+] A methylmalonic acidemia that is characterized by the accumulation of cobalamin in lysosomes which is then unable to synthesize the cofactors adenosylcobalamin (AdoCbl) and methylcobalamin (MeCbl) and that has_material_basis_in homozygous or compound heterozygous mutation in the LMBRD1 gene on chromosome 6q13. [-]
methylmalonic aciduria and homocystinuria type cblE		A methylmalonic acidemia that is characterized by ..[+] A methylmalonic acidemia that is characterized by megaloblastic anemia, lethargy, failure to thrive, developmental delay, intellectual deficit and seizures, has_material_basis_in homozygous or compound heterozygous mutation in the MTRR gene on chromosome 5p15 that causes inborn error of vitamin B12 metabolism. [-]
methylmalonic aciduria and homocystinuria type cblG		n_a
mature T-cell and NK-cell lymphoma	mature T-cell and natural killer cell lymphoma; NK.. [+] mature T-cell and natural killer cell lymphoma; NK-T cell lymphoma [-]	A T-cell non-Hodgkin lymphoma that has_material_ba..[+] A T-cell non-Hodgkin lymphoma that has_material_basis_in mature T lymphocytes and natural killer cells. [-]
mantle cell lymphoma		A B-cell lymphocytic neoplasm due to CD5 positive ..[+] A B-cell lymphocytic neoplasm due to CD5 positive antigen-naive pregerminal center B-cell within the mantle zone that surrounds normal germinal center follicles. [-]
marginal zone lymphoma	marginal zone B-cell lymphoma; marginal zone lymph.. [+] marginal zone B-cell lymphoma; marginal zone lymphoma [-]	A B-cell lymphoma arising from the marginal zone o..[+] A B-cell lymphoma arising from the marginal zone of lymphoid tissues that is characterized by the presence of small to medium sized atypical lymphocytes. [-]
metabolic acidosis		An acquired metabolic disease that characterized b..[+] An acquired metabolic disease that characterized by excessive production of acid. [-]	2 articles
myotonic dystrophy type 2	proximal myotonic myopathy	A myotonic disease that is characterized by myoton..[+] A myotonic disease that is characterized by myotonia and progressive, proximal muscle wasting and weakness affecting the skeletal and smooth muscles of the neck, shoulders, elbows and hips and has_material_basis_in the autosomal dominant inheritance of the CNBP (ZNF9) gene containing an expansion of a CCTG repeat in intron one. [-]	3 articles
midface dysplasia		n_a
mitochondrial complex V (ATP synthase) deficiency nuclear type 1	MC5DN1	A mitochondrial complex V (ATP synthase) deficienc..[+] A mitochondrial complex V (ATP synthase) deficiency that has_material_basis_in mutation in the ATPAF2 gene on chromosome 17p11. [-]
Meckel syndrome	Meckel-Gruber syndrome	A ciliopathy that is characterized by renal cystic..[+] A ciliopathy that is characterized by renal cystic dysplasia, occipital encephalocele, polydactyly (post axial), hepatic developmental defects, and pulmonary hypoplasia. [-]	3 articles
multiple cutaneous and mucosal venous malformations	mucocutaneous venous malformations; VMCM; cutaneom.. [+] mucocutaneous venous malformations; VMCM; cutaneomucosal venous malformation [-]	A vein disease that is characterized by multiple b..[+] A vein disease that is characterized by multiple bluish cutaneous or mucosal venous lesions that has_material_basis_in heterozygous mutation in the TEK gene on chromosome 9p21. [-]
multiple synostoses syndrome		A dysostosis that is characterized by characterize..[+] A dysostosis that is characterized by characterized by multiple joint fusions, usually commencing in the hands, conductive deafness, and characteristic facial features, including a broad, tubular-shaped nose and a thin upper vermilion. [-]
mucopolysaccharidosis IX		A mucopolysaccharidosis characterized by a deficie..[+] A mucopolysaccharidosis characterized by a deficiency in hyaluronidase. [-]
multifocal dystonia		A dystonia that involves two or more unrelated bod..[+] A dystonia that involves two or more unrelated body parts. [-]	1 articles
Muckle-Wells syndrome	MWS; neutrophilic urticaria	A syndrome characterized by episodic skin rash, ar..[+] A syndrome characterized by episodic skin rash, arthralgias, and fever associated with late-onset sensorineural deafness and renal amyloidosis that has_material_basis_in heterozygous mutation in the NLRP3 gene on chromosome 1q44. [-]

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