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Disease	Synonyms	Description
megaloblastic anemia	MGA1 Norwegian type; Grasbeck-Imerslund syndrome; .. [+] MGA1 Norwegian type; Grasbeck-Imerslund syndrome; IGS; Imerslund-Grasbeck syndrome; recessive hereditary megaloblastic anemia 1; RH-MGA1 [-]	A macrocytic anemia that is characterized by inhib..[+] A macrocytic anemia that is characterized by inhibition of DNA synthesis during red blood cell production. [-]
Mobius syndrome	Moebius congenital oculofacial paralysis; Oromandi.. [+] Moebius congenital oculofacial paralysis; Oromandibular-limb hypogenesis spectrum [-]	A facial nerve disease characterized by congenital..[+] A facial nerve disease characterized by congenital, uni- or bilateral, non-progressive facial weakness and limited abduction of the eye(s). [-]
mature cataract	Total or mature cataract; Total, mature senile cat.. [+] Total or mature cataract; Total, mature senile cataract [-]	n_a
malignant renovascular hypertension		n_a
malignant secondary hypertension		n_a
myringitis bullosa hemorrhagica	Bullous myringitis	A tympanic membrane disease that is characterized ..[+] A tympanic membrane disease that is characterized by blisters on the eardrum resulting from infection. [-]
multiple cranial nerve palsy	Multiple cranial nerve palsy (disorder); Multiple .. [+] Multiple cranial nerve palsy (disorder); Multiple cranial nerve palsies NOS (disorder); Multiple cranial nerve palsies (disorder); Multiple cranial nerve palsies [-]	n_a
Morgagni cataract	hypermature cataract	n_a
malignant parietal pleura tumor	primary malignant neoplasm of parietal pleura (dis.. [+] primary malignant neoplasm of parietal pleura (disorder) [-]	n_a
malignant visceral pleura tumor	primary malignant neoplasm of visceral pleura (dis.. [+] primary malignant neoplasm of visceral pleura (disorder) [-]	n_a
median rhomboid glossitis	Persistent tuberculum impar (disorder)	n_a
multiple symmetric lipomatosis	Madelung's neck; Multiple symmetric lipomatosis; c.. [+] Multiple symmetric lipomatosis; Madelung's neck; cervical Symmetrical Lipomatosis; Launois-Bensaude's lipomatosis; LIPODYSTROPHY, CEPHALOTHORACIC; LIPOMATOSIS, FAMILIAL BENIGN CERVICAL [-]	n_a
midline cystocele		n_a
Masters-Allen syndrome	Broad ligament laceration syndrome	A female reproductive system disease that is chara..[+] A female reproductive system disease that is characterized by an excessively mobile uterus secondary to lacerations of the broad and cardinal ligaments, specific tenderness with movement of the cervix and previous untoward obstetrics events, such as premature maternal voluntary efforts, precipate delivery, and forceps delivery. [-]
malignant anus melanoma	malignant melanoma of anus (disorder); anal melano.. [+] malignant melanoma of anus (disorder); anal melanoma [-]	n_a
Marfan syndrome	Marfan's syndrome	A connective tissue disease that is characterized ..[+] A connective tissue disease that is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and subluxation of the lens. [-]
mixed malaria	Malaria fever by more than one parasite; malaria b.. [+] Malaria fever by more than one parasite; malaria by more than one parasite [-]	A malaria that involves infection with more than o..[+] A malaria that involves infection with more than one species of Plasmodium at the same time. [-]
mixed gonadal dysgenesis		n_a
malignant cardiac peripheral nerve sheath neoplasm	MPNST of Heart	n_a
malignant cardiac germ cell tumor	malignant germ cell tumor of the Heart	n_a
multiple intestinal atresia	Multiple gastrointestinal atresias (disorder)	n_a
methylmalonic acidemia	METHYLMALONICACIDURIA, vitamin B12-RESPONSIVE, DUE.. [+] METHYLMALONICACIDURIA, vitamin B12-RESPONSIVE, DUE TO DEFECT IN SYNTHESIS OF ADENOSYLCOBALAMIN--cbl B; METHYLMALONICACIDURIA, vitamin B12-RESPONSIVE, DUE TO DEFECT IN SYNTHESIS OF ADENOSYLCOBALAMIN--cbl A; METHYLMALONICACIDURIA DUE TO METHYLMALONIC CoA MUTASE deficiency; METHYLMALONIC ACIDURIA, VITAMIN B12-RESPONSIVE, DUE TO DEFECT IN SYNTHESIS OF ADENOSYLCOBALAMIN, cblB TYPE; METHYLMALONIC ACIDURIA, VITAMIN B12-RESPONSIVE, DUE TO DEFECT IN SYNTHESIS OF ADENOSYLCOBALAMIN, cblA TYPE; METHYLMALONIC ACIDURIA, mut TYPE; methylmalonic aciduria type cblB; methylmalonic aciduria type cblA; methylmalonic aciduria mut type; METHYLMALONIC ACIDURIA DUE TO METHYLMALONYL-CoA MUTASE DEFICIENCY; methylmalonic aciduria cblB type; methylmalonic aciduria; METHYLMALONIC ACIDEMIA, cblB TYPE; METHYLMALONIC ACIDEMIA, cblA TYPE [-]	An organic acidemia that involves an accumulation ..[+] An organic acidemia that involves an accumulation of methylmalonic acid in the blood. [-]
maleic anhydride allergic asthma	allergic asthma to MA	An allergic asthma that has_allergic_trigger malei..[+] An allergic asthma that has_allergic_trigger maleic anhydride. [-]
mineral metabolism disease		An acquired metabolic disease that is characterize..[+] An acquired metabolic disease that is characterized by abnormal mineral metabolism. [-]
motility-related diarrhea		Motility-related diarrhea is a diarrhea which is c..[+] Motility-related diarrhea is a diarrhea which is caused by the rapid movement of food through the intestines (hypermotility). If the food moves too quickly through the GI tract, there is not enough time for sufficient nutrients and water to be absorbed. [-]
monogenic disease		A genetic disease that is the result of one or mor..[+] A genetic disease that is the result of one or more abnormal alleles and may be dominant (a single copy of the abnormal allele is sufficient to give rise to the disease), semi-dominant, or recessive (requiring both copies of the gene to have an abnormal allele). [-]
mesocestoidiasis		A parasitic helminthiasis infectious disease that ..[+] A parasitic helminthiasis infectious disease that involves parasitic cestode infection caused by Mesocestoides lineatus resulting in nausea, diarrhea, abdominal discomfort and vomiting. [-]
multiple endocrine neoplasia type 2A	MEN2A; multiple endocrine neoplasia II; Sipple syn.. [+] multiple endocrine neoplasia II; MEN2A; Sipple syndrome [-]	An autosomal dominant disease characterized by med..[+] An autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis. [-]
mulibrey nanism	Muscle-Liver-Brain-Eye Nanism; Perheentupa Syndrom.. [+] Muscle-Liver-Brain-Eye Nanism; Perheentupa Syndrome; PERICARDIAL CONSTRICTION AND GROWTH FAILURE [-]	n_a
mucosulfatidosis	multiple sulfatase deficiency disease; Sulfatidosi.. [+] multiple sulfatase deficiency disease; Sulfatidosis, Juvenile, Austin Type [-]	n_a
mevalonic aciduria	Mevalonate Kinase Deficiency	A peroxisomal disease that is characterized by cor..[+] A peroxisomal disease that is characterized by cortical atrophy, microcephaly, dysmorphic facies, muscular hypotonia and intellectual disability and has_material_basis_in mutation in the MVK gene that results in deficiency of mevalonate kinase and impaired cholesterol. biosynthesis. [-]
Muir-Torre syndrome		n_a
monilethrix		n_a
multinodular goiter		A goiter characterized by a multinodular enlargeme..[+] A goiter characterized by a multinodular enlargement of the thyroid gland. [-]
meningovascular neurosyphilis		A tertiary neurosyphilis that results in inflammat..[+] A tertiary neurosyphilis that results in inflammation located_in arteries of the brain or located_in arteries of spinal cord. The infection has_symptom headache, has_symptom neck stiffness, has_symptom dizziness, has_symptom behavioral abnormalities, has _symptom poor concentration, has_symptom memory loss, has _symptom lassitude, has_symptom insomnia, has_symptom blurred vision, has_symptom weakness and wasting of shoulder-girdle and arm muscles, has_symptom slowly progressive leg weakness with urinary or fecal incontinence or both, and has_symptom paralysis of the legs due to thrombosis of spinal arteries. [-]
maturity-onset diabetes of the young	MODY; Mason-type diabetes	A genetic disease that has_material_basis_in mutat..[+] A genetic disease that has_material_basis_in mutations in the MODY genes disrupting insulin production. [-]
muscular dystrophy-dystroglycanopathy type B1	Muscular dystrophy-dystroglycanopathy congenital w.. [+] Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B1; CMD due to dystroglycanopathy [-]	A congenital muscular dystrophy characterized by m..[+] A congenital muscular dystrophy characterized by muscle weakness, cognitive impairment and brain abnormalities and has_material_basis_in mutation to the POMT1 gene that encodes O-mannosyltransferase. [-]
malignant Sertoli-Leydig cell tumor		n_a
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	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	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	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). [-]
methylmalonic aciduria and homocystinuria type cblE		n_a
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 non-Hodgkin lymphoma that has_material_basis_in ..[+] A 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 B-cell lymphoma	marginal zone lymphoma	A B-cell lymphoma that is characterized by initial..[+] A B-cell lymphoma that is characterized by initial formation in the marginal zones of lymph tissue. [-]
metabolic acidosis		An acquired metabolic disease that characterized b..[+] An acquired metabolic disease that characterized by excessive production of acid. [-]
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_physical_basis_in the autosomal dominant inheritance of the CNBP (ZNF9) gene containing an expansion of a CCTG repeat in intron one. [-]

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