Xenbase

Search Diseases

Alphabetic Search:

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

???pagination.result.count???

???pagination.result.page??? ???pagination.result.prev??? 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 ???pagination.result.next???

Disease	Synonyms	Description	Articles
male genital organ vascular disease	vascular disorder of male genital organs	n_a
male infertility		n_a	5 articles
malaria	induced malaria	A parasitic protozoa infectious disease characteri..[+] A parasitic protozoa infectious disease characterized as a vector-borne infectious disease caused by the presence of protozoan parasites of the genus Plasmodium in the red blood cells, transmitted from an infected to an uninfected individual by the bite of anopheline mosquitoes, and characterized by periodic attacks of chills and fever that coincide with mass destruction of blood cells and the release of toxic substances by the parasite at the end of each reproductive cycle. [-]	10 articles
mixed receptive-expressive language disorder		A communication disorder that involves both the re..[+] A communication disorder that involves both the receptive and expressive areas of communication may be affected in any degree, from mild to severe. [-]
myoclonic cerebellar dyssynergia	Dyssynergia cerebellaris myoclonica; progressive c.. [+] Dyssynergia cerebellaris myoclonica; progressive cerebellar tremor [-]	n_a
multiple epiphyseal dysplasia	polyepiphyseal dysplasia	An osteochondrodysplasia that has_material_basis_i..[+] An osteochondrodysplasia that has_material_basis_in defective cartilage mineralization into bone which results in irregular ossification centers of the located in hip or located in knee. The disease has symptom fatigue, has symptom joint pain. [-]
migraine without aura	common migraine	A migraine that is characterized by migraine heada..[+] A migraine that is characterized by migraine headaches that are not accompanied by an aura. [-]
mucopolysaccharidosis		A lysosomal storage disease that involves the accu..[+] A lysosomal storage disease that involves the accumulation of glycosaminoglycans in the tissues and their excretion in the urine. [-]
mucopolysaccharidosis II	Mucopolysaccharidosis, MPS-II; Mucopolysaccharidos.. [+] Mucopolysaccharidosis, MPS-II; Mucopolysaccharidosis, MPS-II (disorder); MPS II - Hunter syndrome; Hunter's syndrome; Hunter syndrome; deficiency of iduronate-2-sulphatase [-]	A mucopolysaccharidosis characterized by a deficie..[+] A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme iduronate sulfatase. [-]
mucopolysaccharidosis VI	MPS VI - Maroteaux-Lamy syndrome; Maroteaux-Lamy s.. [+] MPS VI - Maroteaux-Lamy syndrome; Maroteaux-Lamy syndrome; Maroteaux - Lamy syndrome; arylsulfatase B deficiency; deficiency of N-acetylgalactosamine-4-sulfatase (disorder); deficiency of N-acetylgalactosamine-4-sulfatase [-]	A mucopolysaccharidosis characterized by a deficie..[+] A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme N-acetylgalactosamine 4-sulfatase. [-]
mucopolysaccharidosis III	Mucopolysaccharidosis, MPS-III; MPS IIIB - Sanfili.. [+] Mucopolysaccharidosis, MPS-III; MPS IIIB - Sanfilippo syndrome B; Mucopolysaccharidosis, MPS-III-B; mucopolysaccharidosis type IIIB; mucopolysaccharidosis type IIIA; MPS IIID - Sanfilippo syndrome D; MPS IIIC - Sanfilippo syndrome C; MPS IIIA - Sanfilippo syndrome A; heparan sulfate sulfatase deficiency; N-acetyl-alpha-D-glucosaminidase deficiency; naglu deficiency; Sanfilippo syndrome A; Sanfilippo syndrome B; N-sulphoglucosamine sulphohydrolase deficiency; Sanfilippo's syndrome [-]	A mucopolysaccharidosis characterized by a deficie..[+] A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme resulting in incomplete breakdown of the heparan sulfate sugar chain. [-]
mucopolysaccharidosis I	Mucopolysaccharidosis, MPS-I; MPS I - Hurler syndr.. [+] Mucopolysaccharidosis, MPS-I; MPS I - Hurler syndrome; Mucopolysaccharidosis, type 1; Mucopolysaccharidosis, MPS-I (disorder); Hurler-Scheie syndrome; iduronidase deficiency disease; Lipochondrodystrophy; Hurler syndrome [-]	A mucopolysaccharidosis characterized by a deficie..[+] A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme alpha-L-iduronidase. [-]
mucopolysaccharidosis IV	Mucopolysaccharidosis, MPS-IV; Mucopolysaccharidos.. [+] Mucopolysaccharidosis, MPS-IV; Mucopolysaccharidosis type IVB; Morquio A disease; Mucopolysaccharidosis, MPS-IV-A (disorder); mucopolysaccharidosis type IVA; MPS IV - Morquio syndrome B; MPS IV - Morquio syndrome A; Morquio syndrome A; chondroosteodystrophy; deficiency of chondroitinsulphatase; deficiency of N-acetylgalactosamine-6-sulphatase; galactosamine-6-sulfatase deficiency; Osteochondrodystrophy [-]	A mucopolysaccharidosis characterized by a deficie..[+] A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzymes galactose 6-sulfate sulfatase (Type A) or beta-galactosidase (Type B) needed to break down the keratan sulfate sugar chain. [-]
Miller Fisher syndrome	Miller-Fisher variant of Guillain-Barre syndrome; .. [+] Miller-Fisher variant of Guillain-Barre syndrome; Fisher's syndrome (disorder); 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. [-]
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. [-]
mucocele of salivary gland	Mucous retention cyst of salivary gland; Ranula; S.. [+] Mucous retention cyst of salivary gland; Ranula; Salivary Cyst; Salivary gland mucocele [-]	n_a
mechanical lagophthalmos		n_a
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. [-]
mechanical entropion		n_a
megaesophagus		n_a

???pagination.result.page??? ???pagination.result.prev??? 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 ???pagination.result.next???