Experimental Factor Ontology
926 terms(s) returned
Term Type: | Record: 751 to 800 of 926 Records | Page: 16 of 19, First Previous Next Last | Show Records Per Page |
- multiple endocrine neoplasia type 1
- multiple endocrine neoplasia type 2
- multiple endocrine neoplasia type 2A
- multiple endocrine neoplasia type 2B
- multiple endocrine neoplasia type 4
- multiple epiphyseal dysplasia
- multiple epiphyseal dysplasia due to collagen 9 anomaly
- multiple epiphyseal dysplasia type 1
- multiple epiphyseal dysplasia type 4
- multiple epiphyseal dysplasia type 5
- multiple epiphyseal dysplasia, Al-Gazali type
- multiple epiphyseal dysplasia, Beighton type
- multiple epiphyseal dysplasia, Lowry type
- multiple epiphyseal dysplasia, with miniepiphyses
- multiple epiphyseal dysplasia, with severe proximal femoral dysplasia
- multiple fibroadenoma of the breast
- multiple intestinal atresia
- multiple mitochondrial dysfunctions syndrome 1
- multiple mitochondrial dysfunctions syndrome 2
- multiple mitochondrial dysfunctions syndrome 3
- multiple mitochondrial dysfunctions syndrome 4
- multiple mitochondrial dysfunctions syndrome 6
- multiple polyglandular tumor
- multiple pterygium syndrome
- multiple pterygium-malignant hyperthermia syndrome
- multiple sclerosis
- multiple sclerosis, susceptibility to
- multiple sclerosis, susceptibility to, 5
- multiple sclerosis-ichthyosis-factor VIII deficiency syndrome
- multiple self-healing squamous epithelioma
- multiple synostoses syndrome
- multiple synostoses syndrome 1
- multiple synostoses syndrome 2
- multiple system atrophy 1, susceptibility to
- multiple system atrophy, cerebellar type
- multisystemic smooth muscle dysfunction syndrome
- muscle tissue disorder
- muscle-eye-brain disease
- muscle-eye-brain disease with bilateral multicystic leucodystrophy
- muscular atrophy
- muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome
- muscular dystrophy
- muscular dystrophy, adult-onset, with leukoencephalopathy
- muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome
- muscular dystrophy, congenital, with or without seizures
- muscular dystrophy, congenital, with rapid progression
- muscular dystrophy, limb-girdle, autosomal dominant
- muscular dystrophy, limb-girdle, autosomal dominant 4
- muscular dystrophy, limb-girdle, autosomal recessive 23
- muscular dystrophy, limb-girdle, autosomal recessive 27