Disease Index
9,486 diseasesmitochondrial pyruvate carrier deficiency
human disease
mitochondrial substrate carrier disorder
human disease
mitochondrial trifunctional protein deficiency
medical condition
MeSH: C566945
mitral atresia
human disease
mitral valve agenesis
human disease
mixed autoinflammatory and autoimmune syndrome
human disease
mixed connective tissue disease
collagen disease that is considered an overlap of three diseases, systemic lupus erythematosus, scleroderma, and polymyositis with very high titers of circulating antinuclear antibody to a ribonucleoprotein antigen
MeSH: D008947
mixed cryoglobulinemia type III
mixed cystic lymphatic malformation
human disease
mixed dermis disorder
human disease
mixed functioning pituitary adenoma
human disease
mixed germ cell cancer
germ cell cancer that occurs in many forms
mixed germ cell tumor of central nervous system
malignant germ cell tumor of the central nervous system characterized by the presence of at least two types of germ cell neoplasia
mixed gonadal dysgenesis X0/XY
intersex variation
MeSH: D006060
mixed hyperlipidemia
medical condition
ICD: E78.4
mixed oligodendroglioma-astrocytoma
Human disease
mixed phenotype acute leukemia
acute leukemia in which the blasts lack sufficient evidence to classify as myeloid or lymphoid or they have morphologic and/or immunophenotypic characteristics of both myeloid and lymphoid cells. (WHO, 2001)
mixed sclerosing bone dystrophy with extra-skeletal manifestations
human disease
mixed type thymoma
Human disease
mixed-type autoimmune hemolytic anemia
rare autoimmune disease
Miyoshi muscular dystrophy
distal muscular dystrophy 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
MeSH: C537480
MMEP syndrome
; 6q21) has been shown to play a causative role in MMEP, although this was not confirmed in recent studies
MeSH: C537686
Mobius syndrome
rare disease
MeSH: D020331
moderate multiminicore disease with hand involvement
human disease
moderately severe hemophilia A
Moderately severe hemophilia A is a form of hemophilia A (see this term) characterized by factor VIII deficiency leading to abnormal bleeding as a result of minor injuries, or following surgery or tooth extraction
Moderately severe hemophilia b
Moderately severe hemophilia B is a form of hemophilia B (see this term) characterized by factor IX deficiency leading to abnormal bleeding as a result of minor injuries, or following surgery or tooth extraction
moderately-differentiated thymic neuroendocrine carcinoma
human disease
Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome
This syndrome is characterized by the association of MC6bius syndrome (congenital facial palsy with impaired ocular abduction; see this term) with peripheral axonal neuropathy and hypogonadotropic hypogonadism
MeSH: C535806
Mohr syndrome
molybdenum cofactor deficiency
metal metabolism disease characterized by encephalopathy that worsens over time resulting from the absence of molybdenum cofactor which leads to accumulation of toxic levels of sulphite and neurological damage