Experimental Factor Ontology
157 terms(s) returned
Term Type: | Record: 101 to 150 of 157 Records | Page: 3 of 4, First Previous Next Last | Show Records Per Page |
- Mirror polydactyly - vertebral segmentation - limbs defects
- Miscellaneous movement disorder due to genetic neurodegenerative disease
- Mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy
- Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies
- Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency
- Mitochondrial disease with dilated cardiomyopathy
- Mitochondrial disease with eye involvement
- Mitochondrial disease with hypertrophic cardiomyopathy
- Mitochondrial disease with peripheral neuropathy
- Mitochondrial disorder due to a defect in assembly or maturation of the respiratory chain complexes
- Mitochondrial disorder due to a defect in mitochondrial protein synthesis
- Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency
- Mitochondrial myopathy
- Mitochondrial myopathy - lactic acidosis - deafness
- Mitochondrial myopathy and sideroblastic anemia
- Mitochondrial non-syndromic sensorineural deafness
- Mitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposure
- Mitochondrial oxidative phosphorylation disorder due to a duplication of mitochondrial DNA
- Mitochondrial oxidative phosphorylation disorder due to a large-scale single deletion of mitochondrial DNA
- Mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA
- Mitochondrial oxidative phosphorylation disorder due to mitochondrial DNA anomalies
- Mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies
- Mitochondrial oxidative phosphorylation disorder with no known mechanism
- Moebius syndrome
- Mohr-Tranebjaerg syndrome
- Monoamine oxidase A deficiency
- Monogenic disease with epilepsy
- Monosomy 18p
- Monosomy 22q13
- Monosomy 5p
- Monosomy 9p
- Monosomy Xp21
- Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism
- Mucocutaneous venous malformations
- Mucopolysaccharidosis with skin involvement
- Multinodular goiter - cystic kidney - polydactyly
- Multiple congenital anomalies - hypotonia - seizures syndrome
- Multiple congenital anomalies-hypotonia-seizures syndrome type 2
- Multiple non-ossifying fibromatosis
- Multiple osteochondromas
- Multiple sclerosis - ichthyosis - factor VIII deficiency
- Multiple sulfatase deficiency
- Multiple ventricular septal defects
- Muscle filaminopathy
- Muscular atrophy - ataxia - retinitis pigmentosa - diabetes mellitus
- Muscular dystrophy - white matter spongiosis
- Muscular hypertrophy - hepatomegaly - polyhydramnios
- Muscular pseudohypertrophy - hypothyroidism
- Musculoskeletal disease with cataract
- Myasthenic syndrome with eye involvement