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Disease	Synonyms	Description	Articles
Meckel syndrome 2	Meckel-Gruber syndrome, type 2; MKS2;	A Meckel syndrome that has_material_basis_in an au..[+] A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TMEM216 gene on chromosome 11q12.2. [-]
Meckel syndrome 3	Meckel-Gruber syndrome, type 3; MKS3;	A Meckel syndrome that has_material_basis_in an au..[+] A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TMEM67 gene on chromosome 8q22.1. [-]
Meckel syndrome 4	Meckel-Gruber syndrome, type 4; MKS4;	A Meckel syndrome that has_material_basis_in an au..[+] A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the CEP290 gene on chromosome 12q21.32. [-]
Meckel syndrome 5	Meckel-Gruber syndrome, type 5; MKS5;	A Meckel syndrome that has_material_basis_in an au..[+] A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the RPGRIP1L gene on chromosome 16q12.2. [-]
Meckel syndrome 6	Meckel-Gruber syndrome, type 6; MKS6;	A Meckel syndrome that has_material_basis_in an au..[+] A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the CC2D2A gene on chromosome 4p15.32. [-]	1 articles
Meckel syndrome 7	MKS7; Meckel-Gruber syndrome, type 7;	A Meckel syndrome that has_material_basis_in an au..[+] A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the NPHP3 gene on chromosome 3q22.1. [-]
Meckel syndrome 8	Meckel-Gruber syndrome, type 8; MKS8;	A Meckel syndrome that has_material_basis_in an au..[+] A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TCTN2 gene on chromosome 12q24.31. [-]
Meckel's diverticulitis	Meckel diverticulitis; Meckel's diverticulitis (di.. [+] Meckel diverticulitis; Meckel's diverticulitis (disorder); [-]	A diverticulits characterized by the inflammation ..[+] A diverticulits characterized by the inflammation of a congenital diverticulum, which is a slight bulge of the small intestine present at birth. [-]
Meckel's diverticulum	Meckel Diverticulum; Persistent vitelline duct;	A physical disorder that is characterized by a con..[+] A physical disorder that is characterized by a congenital abnormality characterized by the outpouching or sac formation in the ileum. [-]
Meckel's diverticulum cancer	malignant neoplasm of Meckel's diverticulum; Mecke.. [+] malignant neoplasm of Meckel's diverticulum; Meckel diverticulum cancer; [-]	An ileum cancer originating from Meckel's divertic..[+] An ileum cancer originating from Meckel's diverticulum. [-]
Meesmann corneal dystrophy	MECD; juvenile hereditary epithelial dystrophy; St.. [+] MECD; juvenile hereditary epithelial dystrophy; Stocker-Holt dystrophy; [-]	An epithelial and subepithelial dystrophy that is ..[+] An epithelial and subepithelial dystrophy that is characterized by the formation of tiny round cysts in the corneal epithelium. [-]
Meesmann corneal dystrophy 1		A Messmann corneal dystrophy that is characterized..[+] A Messmann corneal dystrophy that is characterized by the presence of multitudinous microcysts within the anterior epithelium and that has_material_basis_in heterozygous mutation in the KRT12 gene on chromosome 17q21. [-]
Meesmann corneal dystrophy 2		A Messmann corneal dystrophy that is characterized..[+] A Messmann corneal dystrophy that is characterized by fragility of the anterior corneal epithelium and the presence of intraepithelial microcysts and that has_material_basis_in heterozygous mutation in the KRT3 gene on chromosome 12q13. [-]
Meester-Loeys syndrome	MRLS;	A syndrome characterized by early-onset aortic ane..[+] A syndrome characterized by early-onset aortic aneurysm and dissection in hemizygous males and variable presentation from unaffected to fatal aortic dissection in heterozygous females, as well as facial dysmorphism, connective tissue anomalies, and features of Loeys-Dietz syndrome that has_material_basis_in mutation in BGN on chromosome Xq28. [-]
Meier-Gorlin syndrome	ear-patella-short stature syndrome;	A syndrome that is characterized by bilateral unde..[+] A syndrome that is characterized by bilateral underdevelopment of the external ear, short stature, absent or underdeveloped patellae and severe prenatal and postnatal growth retardation. [-]
Meige syndrome		A cranio-facial dystonia that is accompanied by bl..[+] A cranio-facial dystonia that is accompanied by blepharospasm. [-]
Melkersson-Rosenthal syndrome	Melkersson's syndrome; Cheilitis granulomatosa of .. [+] Melkersson's syndrome; Cheilitis granulomatosa of Mescher-Melkersson-Rosenthal; [-]	n_a
Melnick-Needles syndrome	Melnick-Needles osteodysplasty; MNS; osteodysplast.. [+] Melnick-Needles osteodysplasty; MNS; osteodysplasty of Melnick and Needles; [-]	An otopalatodigital syndrome spectrum disorder cha..[+] An otopalatodigital syndrome spectrum disorder characterized by short stature, facial dysmorphism, osseous abnormalities involving the majority of the axial and appendicular skeleton resulting in impaired speech and masticatory problems that has_material_basis_in heterozygous or hemizygous mutation in the FLNA gene on chromosome Xq28. [-]
Meniere's disease	Meniere disease; Mnire's vertigo; Otogenic vertigo.. [+] Meniere disease; Mnire's vertigo; Otogenic vertigo; [-]	A vestibular disease characterized by vertigo, low..[+] A vestibular disease characterized by vertigo, low-pitched tinnitus and hearing loss. [-]
Menkes disease	COPPER TRANSPORT DISEASE; Menkes kinky-hair syndro.. [+] COPPER TRANSPORT DISEASE; Menkes kinky-hair syndrome; steely hair syndrome; [-]	n_a
Merkel cell carcinoma	Trabecular adenocarcinoma (morphologic abnormality.. [+] Trabecular adenocarcinoma (morphologic abnormality); Trabecular adenocarcinoma; trabecular carcinoma; [-]	n_a
Middle East respiratory syndrome		A Coronavirus infectious disease that is character..[+] A Coronavirus infectious disease that is characterized by severe respiratory illness, including fever, cough, and shortness of breath and that has_material_basis_in MERS-CoV. [-]
Mikulicz disease	Mikulicz's disease; IgG4-related dacryoadenitis an.. [+] Mikulicz's disease; IgG4-related dacryoadenitis and sialadenitis; [-]	An autoimmune disease that is characterized by chr..[+] An autoimmune disease that is characterized by chronic enlargement of the glands of the head and neck, has_symptom lumps of the face and neck, dry eyes, dry mouth, and intermittent fever, and is often associated with an underlying autoimmune disorder, hematologic malignancy, tuberculosis infection, or syphilis infection. [-]
Miles-Carpenter syndrome	mental retardation, X-linked, syndromic 4; MRXS4; .. [+] mental retardation, X-linked, syndromic 4; MRXS4; MCS; X-linked intellectual disability, Miles-Carpenter type; mental retardation, X-linked, with congenital contractures and low fingertip arches; [-]	A syndromic X-linked intellectual disability chara..[+] A syndromic X-linked intellectual disability characterized by severe intellectual deficit, microcephaly, exotropia, distal muscle wasting and low digital arches that has_material_basis_in variation in chromosomal region Xq13-q22. [-]
Miller Fisher syndrome	Fisher's syndrome (disorder); Miller-Fisher varian.. [+] Fisher's syndrome (disorder); Miller-Fisher variant of Guillain-Barre syndrome; Fisher's syndrome; [-]	A Guillain-Barre syndrome that manifests as a desc..[+] A Guillain-Barre syndrome that manifests as a descending paralysis. It usually affects the eye muscles first and presents with the triad of ophthalmoplegia, ataxia, and areflexia. [-]
Miller-Dieker lissencephaly syndrome	MDS; Miller-Dieker syndrome;	A syndrome characterized by classical lissencephal..[+] A syndrome characterized by classical lissencephaly and distinct facial features and has_material_basis_in submicroscopic deletions of 17p13.3, including the LIS1 gene. [-]	1 articles
Mitchell syndrome		A peroxisomal disease characterized by progressive..[+] A peroxisomal disease characterized by progressive episodic demyelination, sensorimotor polyneuropathy, and hearing loss that has_material_basis_in heterozygous mutation in the ACOX1 gene on chromosome 17q25.1. [-]
Miura type epiphyseal chondrodysplasia	ECDM; tall stature-scoliosis-macrodactyly of the g.. [+] ECDM; tall stature-scoliosis-macrodactyly of the great toes syndrome; tall stature-scoliosis-macrodactyly of the halluces syndrome; [-]	A bone developmental disease characterized by tall..[+] A bone developmental disease characterized by tall stature, scoliosis and macrodactyly of the great toes that has_material_basis_in heterozygous mutation in the NPR2 gene on chromosome 9p13. [-]
Miyoshi muscular dystrophy	Miyoshi myopathy;	A distal myopathy that is characterized by autosom..[+] A distal myopathy that is characterized by autosomal recessive inheritance of distal muscle weakness in the upper and lower limbs that spares the intrinsic muscles of the hands and has onset in young adulthood. [-]
Miyoshi muscular dystrophy 2	Miyoshi myopathy 2; MMD2;	A Miyoshi muscular dystrophy characterized by asym..[+] A Miyoshi muscular dystrophy characterized by asymmetric presentation of muscle weakness and atrophy that has_material_basis_in a locus on chromosome 10. [-]
Miyoshi muscular dystrophy 3	Miyoshi myopathy 3; MMD3;	A Miyoshi muscular dystrophy that has_material_bas..[+] A Miyoshi muscular dystrophy that has_material_basis_in mutation in the ANO5 gene on chromosome 11p14. [-]
Mobitz type II atrioventricular block	Mobitz II atrioventricular block; Mobitz type II a.. [+] Mobitz II atrioventricular block; Mobitz type II atrioventricular block (disorder); Mobitz (type) II atrioventricular block; [-]	n_a
Moebius syndrome	Moebius congenital oculofacial paralysis; Oromandi.. [+] Moebius congenital oculofacial paralysis; Oromandibular-limb hypogenesis spectrum; Mobius syndrome; [-]	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). [-]
Monckeberg arteriosclerosis		n_a
Mononen-Karnes-Senac syndrome	Mononen type brachydactyly; short and abducted thu.. [+] Mononen type brachydactyly; short and abducted thumbs and great toes; [-]	A brachydactyly characterized by short, abducted t..[+] A brachydactyly characterized by short, abducted thumbs and great toes. [-]
Mooren's ulcer	Mooren ulcer;	A corneal ulcer that is characterized by painful p..[+] A corneal ulcer that is characterized by painful peripheral corneal ulceration, sterile limbal inflammation, and episcleral and conjunctival edema. [-]
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. [-]
Mowat-Wilson syndrome	microcephaly, mental retardation, and distinct fac.. [+] microcephaly, mental retardation, and distinct facial featrues, with or without Hirschprung disease; Hirschsprung disease mental retardation syndrome; [-]	A syndrome characterized by distinctive facial fea..[+] A syndrome characterized by distinctive facial features, intellectual disability, delayed development, Hirschsprung disease and has_material_basis_in de novo heterozygous mutation in the ZEB2 gene on chromosome 2q22. [-]
Moyamoya disease	progressive intracranial arterial occlusion;	A cerebral arterial disease characterized by const..[+] A cerebral arterial disease characterized by constriction of certain arteries at the base of the brain. Blood flow is blocked by the constriction and also by blood clots. [-]
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. [-]
Muenke Syndrome	FGFR3-related craniosynostosis;	A craniosyntosis characterized by autosomal domina..[+] A craniosyntosis characterized by autosomal dominant inheritance, uni- or bicoronal synostosis, macrocephaly, midfacial hypoplasia, and developmental delay that has_material_basis_in a pro250 to agr (P250R) heterozygous mutation in the FGFR3 gene on chromosome 4p16.3. [-]
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. [-]
Mulchandani-Bhoj-Conlin syndrome	maternal uniparental disomy of chromosome 20; mate.. [+] maternal uniparental disomy of chromosome 20; maternal UPD(20); MBCS; UPD(20)mat; [-]	A syndrome characterized by prenatal growth restri..[+] A syndrome characterized by prenatal growth restriction, severe short stature with proportional head circumference, and profound feeding difficulty that has_material_basis_in heterozygous mutation in an imprinting region on chromosome 20q11-q13. [-]
Mullegama-Klein-Martinez syndrome	MKMS; X-linked neurodevelopmental disorder with cr.. [+] MKMS; X-linked neurodevelopmental disorder with craniofacial abnormalities; NEDXCF; [-]	A syndromic X-linked intellectual disability chara..[+] A syndromic X-linked intellectual disability characterized by global developmental delay with impaired intellectual development and poor speech and commonly associated with ear abnormalities, hearing loss, and dysmorphic facial features that has_material_basis_in heterozygous or hemizygous mutation in the STAG2 gene on chromosome Xq25. [-]
Mullerian aplasia and hyperandrogenism	Mullerian duct failure and hyperandrogenism; WNT4 .. [+] Mullerian duct failure and hyperandrogenism; WNT4 deficiency; [-]	A disorder of sexual development characterized by ..[+] A disorder of sexual development characterized by primary amenorrhea, an underdeveloped or absent uterus, and clinical hyperandrogenism that has_material_basis_in heterozygous mutation in the WNT4 gene on chromosome 1p36.12. [-]
Munchausen by proxy		A factitious disorder that involves a care giver's..[+] A factitious disorder that involves a care giver's deliberate exaggeration, fabrication, and/or induce physical, psychological, behavioral, and/or mental health problems in others. [-]
Murray Valley encephalitis	Australian encephalitis; Australian X disease;	A viral infectious disease that results_in inflamm..[+] A viral infectious disease that results_in inflammation located_in brain, has_material_basis_in Murray Valley encephalitis virus, which is transmitted_by Culex annulirostris mosquitoes. The infection has_symptom fever, has_symptom headache, has_symptom nausea, has_symptom vomiting, has_symptom drowsiness, has_symptom confusion, has_symptom fitting, and has_symptom weakness. [-]
Mycobacterium avium complex disease	Infection due to Mycobacterium intracellulare; Inf.. [+] Infection due to Mycobacterium intracellulare; Infection due to Mycobacterium intracellulare (disorder); MAC disease; Mycobacterium avium Complex; Mycobacterium Avium Infection; [-]	A primary bacterial infectious disease that result..[+] A primary bacterial infectious disease that results_in infection, has_material_basis_in Mycobacterium avium complex (MAC), which is transmitted_by inhalation or transmitted_by ingestion of via the respiratory or gastrointestinal tract respectively. The bacteria cause disseminated infection in HIV infected people, while pulmonary disease in immunocompetent persons. [-]
Mycoplasma pneumoniae pneumonia	cold agglutinin positive pneumonia; Mycoplasmal pn.. [+] cold agglutinin positive pneumonia; Mycoplasmal pneumonia; Pneumonia due to Eaton's agent; Pneumonia due to Mycoplasma pneumoniae; Pneumonia due to Mycoplasma pneumoniae (disorder); Mycoplasma pneumonia; [-]	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. [-]
N syndrome	NSX;	A syndrome that is characterized by intellectual d..[+] A syndrome that is characterized by intellectual disability, deafness, ocular abnormalities, T-cell leukemia, cryptorchidism, hypospadias and spasticity. [-]

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