Disease Index
9,486 diseasescombined oxidative phosphorylation deficiency 24
human disease
combined oxidative phosphorylation deficiency 29
human disease
combined oxidative phosphorylation deficiency 39
human disease
combined oxidative phosphorylation deficiency 4
human disease
combined oxidative phosphorylation deficiency 7
human disease
combined oxidative phosphorylation deficiency 8
human disease
combined oxidative phosphorylation deficiency 9
human disease
combined pancreatic lipase-colipase deficiency
Combined pulmonary fibrosis and emphysema
medical condition
combined vitamin K-dependent clotting factors deficiency
MeSH: C564741
commissural lip fistula
human disease
common mesentery
human disease
common variable immunodeficiency
immune disorder
MeSH: D017074
communicating congenital bronchopulmonary-foregut malformation
human disease
complement 2 deficiency
human disease
complement 3 deficiency
human disease
MeSH: C565169
complement component 4a deficiency
Human disease
MeSH: C565167
complement component 4b deficiency
Human disease
complement component 5 deficiency
Human disease
complement component 6 deficiency
Human disease
complement component 7 deficiency
Human disease
complement component 9 deficiency
Human disease
MeSH: C565165
complement factor I deficiency
Human disease
MeSH: C572568
complete androgen insensitivity syndrome
intersex variation where one has no response to androgens and is born with a vulva and clitoris
ICD: E34.1
complete atrioventricular canal
MeSH: C535974
complete atrioventricular canal-left heart obstruction syndrome
human disease
complete atrioventricular canal-tetralogy of fallot syndrome
human disease
complete atrioventricular canal-ventricle hypoplasia syndrome
human disease
complete cryptophthalmia
human disease
complete hydatidiform mole