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Disease	Synonyms	Description	Articles	Phenotypes
mesenteric vascular occlusion		n_a
Mycoplasma pneumoniae pneumonia	Mycoplasmal pneumonia; Mycoplasma pneumonia; cold .. [+] Mycoplasma pneumonia; Mycoplasmal pneumonia; cold agglutinin positive pneumonia; Pneumonia due to Eaton's agent; Pneumonia due to Mycoplasma pneumoniae; Pneumonia due to Mycoplasma pneumoniae (disorder) [-]	A bacterial pneumonia that is caused by the bacter..[+] A bacterial pneumonia that is caused by the bacterial species Mycoplasma pneumoniae. The symptoms include chest pain, chills, dry cough which is not bloody, excessive sweating, fever, headache and sore throat. [-]
megaloblastic anemia	MGA1 Norwegian type; megaloblastic anaemia; Grasbe.. [+] megaloblastic anaemia; MGA1 Norwegian type; Grasbeck-Imerslund syndrome; IGS; RH-MGA1; Imerslund-Grasbeck syndrome; recessive hereditary megaloblastic anaemia 1; recessive hereditary megaloblastic anemia 1 [-]	A macrocytic anemia that is characterized by inhib..[+] A macrocytic anemia that is characterized by inhibition of DNA synthesis during red blood cell production. [-]
Moebius syndrome	Mobius syndrome; Moebius congenital oculofacial pa.. [+] Mobius syndrome; 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 [-]	A senile cataract that is characterized by full wh..[+] A senile cataract that is characterized by full white or brunescent opacification of the lens of the eye such that the red reflex is obscured. It is a later stage of senile cataracts and is caused by a multifactorial etiology related to aging. [-]
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; Multiple cranial ner.. [+] Multiple cranial nerve palsy; Multiple cranial nerve palsies NOS (disorder); Multiple cranial nerve palsy (disorder); Multiple cranial nerve palsies (disorder); Multiple cranial nerve palsies [-]	n_a
Morgagni cataract	hypermature cataract	A senile cataract that is characterized by dense w..[+] A senile cataract that is characterized by dense white opacification of the lens and milky fluid in the lens capsule such that the dense nucleus of the lens sinks in the surrounding fluid. It is the late stage of senile cataracts and is caused by a multifactorial etiology related to aging. [-]
malignant parietal pleura tumor	primary malignant neoplasm of parietal pleura (dis.. [+] primary malignant neoplasm of parietal pleura (disorder); primary malignant neoplasm of parietal pleura [-]	n_a
malignant visceral pleura tumor	primary malignant neoplasm of visceral pleura (dis.. [+] primary malignant neoplasm of visceral pleura (disorder); primary malignant neoplasm of visceral pleura [-]	n_a
median rhomboid glossitis	Persistent tuberculum impar (disorder); Persistent.. [+] Persistent tuberculum impar (disorder); Persistent tuberculum impar [-]	n_a
multiple symmetric lipomatosis	multiple symmetrical lipomatosis; Madelung's neck; .. [+] Madelung's neck; multiple symmetrical lipomatosis; Multiple symmetric lipomatosis; LIPODYSTROPHY, CEPHALOTHORACIC; LIPOMATOSIS, FAMILIAL BENIGN CERVICAL; cervical Symmetrical Lipomatosis; Launois-Bensaude's lipomatosis [-]	n_a
midline cystocele		A prolapse of the female genital organ that is cha..[+] A prolapse of the female genital organ that is characterized by the descent of the bladder causing a bulge in the midline anterior vaginal wall. [-]
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; malignant melanoma of .. [+] malignant melanoma of anus; 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. [-]	3 articles
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		A gonadal dysgenesis that is characterized by prog..[+] A gonadal dysgenesis that is characterized by progressive loss of primordial cells on the developing glands of an embryo, leading to extremely hypoplastic and dysfuctioning gonads resulting in one differentiated gonad and either a streak gonad or streak testis. [-]
malignant cardiac peripheral nerve sheath neoplasm	MPNST of Heart	n_a
malignant cardiac germ cell tumor	malignant germ cell tumour of the Heart; malignant.. [+] malignant germ cell tumour of the Heart; malignant cardiac germ cell tumour; malignant germ cell tumor of the Heart [-]	n_a
multiple intestinal atresia	Multiple gastrointestinal atresias; MEDDRA:1002821.. [+] Multiple gastrointestinal atresias; MEDDRA:10028210; Multiple gastrointestinal atresias (disorder); familial intestinal polyatresia syndrome; GIDID; gastrointestinal defects and immunodeficiency syndrome [-]	An intestinal disease characterized by the presenc..[+] An intestinal disease characterized by the presence of numerous atresic segments in the small and large intestines that has_material_basis_in homozygous or compound heterozygous mutation in the TTC7A gene on chromosome 2p21. [-]
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; 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 DUE TO METHYLMALONYL-CoA MUTASE DEFICIENCY; methylmalonic aciduria cblB type; methylmalonic aciduria; METHYLMALONIC ACIDEMIA, cblB TYPE; METHYLMALONIC ACIDEMIA, cblA TYPE; METHYLMALONICACIDURIA DUE TO METHYLMALONIC CoA MUTASE deficiency; methylmalonic aciduria mut type [-]	An organic acidemia that involves an accumulation ..[+] An organic acidemia that involves an accumulation of methylmalonic acid in the blood. [-]
melphalan allergy	Alkeran allergy	A drug allergy that has_allergic_trigger melphalan..[+] A drug allergy that has_allergic_trigger melphalan. [-]
mineral metabolism disease		An acquired metabolic disease that is characterize..[+] An acquired metabolic disease that is characterized by abnormal mineral metabolism. [-]	6 articles
motility-related diarrhea		A diarrhea which is caused by the rapid movement o..[+] 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). [-]	281 articles	213 matches
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	multiple endocrine neoplasia II; MEN2A; Sipple syn.. [+] MEN2A; multiple endocrine neoplasia II; Sipple syndrome [-]	A multiple endocrine neoplasia characterized by me..[+] A multiple endocrine neoplasia characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis. [-]
mulibrey nanism	MUL; Mulibrey growth disorder; Muscle-Liver-Brain-.. [+] Mulibrey growth disorder; MUL; Muscle-Liver-Brain-Eye Nanism; Perheentupa Syndrome; PERICARDIAL CONSTRICTION AND GROWTH FAILURE [-]	A syndrome that is characterized by global growth ..[+] A syndrome that is characterized by global growth retardation of the muscle, liver, brain and eyes as well as constrictive pericarditis and has_material_basis_in mutations in the TRIM37 gene. [-]
mucosulfatidosis	multiple sulfatase deficiency disease; Sulfatidosi.. [+] multiple sulfatase deficiency disease; Sulfatidosis, Juvenile, Austin Type [-]	A sphingolipidosis that is characterized by leukod..[+] A sphingolipidosis that is characterized by leukodystrophy, ichthyosis, skeletal abnormalities and shortened life expectancy and has_material_basis_in mutation in the SUMF1 gene that results in deficiency in multiple sulfatase enzymes. [-]
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		A Lynch syndrome that is characterized by a propen..[+] A Lynch syndrome that is characterized by a propensity to develop cancers of the gastrointestinal tract, genitourinary tract, and skin that has_material_basis_in mutations in DNA mismatch repair genes. [-]
monilethrix		A hair disease that is characterized by short, eas..[+] A hair disease that is characterized by short, easily broken hair that results in alopecia and has_material_basis_in mutations in genes for type II hair cortex keratins. [-]
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	Mason-type diabetes; MODY	A diabetes mellitus that has_material_basis_in aut..[+] A diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutations in the MODY genes impacting beta-cell function, typically occurring before 25 years of age and caused by primary insulin secretion defects. [-]	3 articles
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. [-]
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

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