Human Disease Ontology
1127 terms(s) returned
| Term Type: | Record: 701 to 750 of 1127 Records | Page: 15 of 23, First Previous Next Last | Show Records Per Page |
- mitochondrial complex IV deficiency nuclear type 14
- mitochondrial complex IV deficiency nuclear type 15
- mitochondrial complex IV deficiency nuclear type 16
- mitochondrial complex IV deficiency nuclear type 17
- mitochondrial complex IV deficiency nuclear type 18
- mitochondrial complex IV deficiency nuclear type 19
- mitochondrial complex IV deficiency nuclear type 2
- mitochondrial complex IV deficiency nuclear type 20
- mitochondrial complex IV deficiency nuclear type 21
- mitochondrial complex IV deficiency nuclear type 22
- mitochondrial complex IV deficiency nuclear type 23
- mitochondrial complex IV deficiency nuclear type 3
- mitochondrial complex IV deficiency nuclear type 4
- mitochondrial complex IV deficiency nuclear type 6
- mitochondrial complex IV deficiency nuclear type 7
- mitochondrial complex IV deficiency nuclear type 8
- mitochondrial complex IV deficiency nuclear type 9
- mitochondrial complex V (ATP synthase) deficiency
- mitochondrial complex V (ATP synthase) deficiency mitochondrial type 1
- mitochondrial complex V (ATP synthase) deficiency nuclear type 1
- mitochondrial complex V (ATP synthase) deficiency nuclear type 2
- mitochondrial complex V (ATP synthase) deficiency nuclear type 3
- mitochondrial complex V (ATP synthase) deficiency nuclear type 4
- mitochondrial complex V (ATP synthase) deficiency nuclear type 4A
- mitochondrial complex V (ATP synthase) deficiency nuclear type 4B
- mitochondrial complex V (ATP synthase) deficiency nuclear type 5
- mitochondrial complex V (ATP synthase) deficiency nuclear type 6
- mitochondrial complex V (ATP synthase) deficiency nuclear type 7
- mitochondrial encephalomyopathy
- mitochondrial inheritance
- mitochondrial metabolism disease
- mitochondrial myopathy
- mitochondrial nonsyndromic sensorineural deafness
- mitochondrial pyruvate carrier deficiency
- mitochondrial short-chain enoyl-CoA hydratase 1 deficiency
- mitochondrial trifunctional protein deficiency
- mitochondrial trifunctional protein deficiency 1
- mitochondrial trifunctional protein deficiency 2
- mitochondrial type mitochondrial complex I deficiency
- mitochondrial type mitochondrial complex I deficiency 1
- mitral valve
- mitral valve disease
- mitral valve insufficiency
- mitral valve prolapse
- mitral valve stenosis
- mixed astrocytoma-ependymoma
- mixed astrocytoma-ependymoma-oligodendroglioma
- mixed cell adenoma
- mixed cell type adenoma of parathyroid
- mixed cell type cancer
