Disease Index
9,486 diseasesmucopolysaccharidosis
lysosomal storage disease that involves the accumulation of glycosaminoglycans in the tissues and their excretion in the urine
MeSH: D009083
mucopolysaccharidosis I
lysosomal storage disease
MeSH: D008059
mucopolysaccharidosis II
mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme iduronate sulfatase
MeSH: D016532
mucopolysaccharidosis IX
mucopolysaccharidosis characterized by a deficiency in hyaluronidase
MeSH: C563209
mucopolysaccharidosis type 2, attenuated form
mucopolysaccharidosis type 2, severe form
mucopolysaccharidosis type 6, rapidly progressing
human disease
mucopolysaccharidosis type 6, slowly progressing
human disease
mucopolysaccharidosis type IIIA
human disease
mucopolysaccharidosis type IIIB
human disease
mucopolysaccharidosis type IIIC
human disease
mucopolysaccharidosis type IIID
human disease
mucopolysaccharidosis type IVA
human disease
mucopolysaccharidosis type IVB
human disease
mucopolysaccharidosis VI
lysosomal storage disease
ICD: E76.2MeSH: D009087
mucopolysaccharidosis with skin involvement
human disease
mucormycosis
fungal infection by the order Mucorales
ICD: B46.0MeSH: D009091
mucosal melanoma
melanoma that has material basis in melanocytes located in mucosal membranes lining the respiratory, gastrointestinal and urogenital tract
ICD: C43.9
mucosulfatidosis
lysosomal storage disease
MeSH: D052517
mucous membrane pemphigoid
Mueller Weiss syndrome
osteonecrotic disease of the foot
Muenke syndrome
human disease
MeSH: C537369
Muir-Torre syndrome
Human disease
MeSH: D055653
mulibrey nanism
Human disease
MeSH: D050336
Müllerian agenesis
congenital atypical development of Müllerian ducts
ICD: Q51.0MeSH: C567186
mullerian aplasia
human disease
MeSH: C537371
mullerian derivatives-lymphangiectasia-polydactyly syndrome
MeSH: C536478
mullerian duct anomalies-limb anomalies syndrome
MeSH: C537155
multicentric carpo-tarsal osteolysis with or without nephropathy
human disease
MeSH: C567171
multicentric Castleman disease
Castleman disease characterized by systemic inflammatory symptoms, polyclonal lymphoproliferation, cytopenias, and multiple organ system dysfunction caused by a cytokine storm often including interleukin-6
MeSH: C537372