Experimental Factor Ontology
157 terms(s) returned
| Term Type: | Record: 1 to 50 of 157 Records | Page: 1 of 4, First Previous Next Last | Show Records Per Page |
- MACS syndrome
- MEGDEL syndrome
- MELAS
- MERRF
- MITF-related melanoma and renal cell carcinoma predisposition syndrome
- MODY
- MURCS association
- MYH9-related disease
- Macrocephaly - immune deficiency - anemia
- Macrocephaly - short stature - paraplegia
- Macrocephaly - spastic paraplegia - dysmorphism
- Macrosomia - microphthalmia - cleft palate
- Macrostomia - preauricular tags - external ophthalmoplegia
- Macrothrombocytopenia with mitral valve insufficiency
- Macular coloboma - cleft palate - hallux valgus
- Male hypergonadotropic hypogonadism - intellectual disability - skeletal anomalies
- Male infertility due to gonadal dysgenesis
- Male infertility due to gonadal dysgenesis or sperm disorder
- Male infertility due to large-headed multiflagellar polyploid spermatozoa
- Male infertility due to obstructive azoospermia of genetic origin
- Male infertility due to sperm disorder
- Male infertility due to sperm motility disorder
- Male infertility with spermatogenesis disorder
- Male infertility with spermatogenesis disorder due to single gene mutation
- Malformation of the neurenteric canal, spinal cord and column
- Malformation syndrome with connective tissue involvement
- Malformation syndrome with hamartosis
- Malformation syndrome with skin/mucosae involvement
- Malformative syndrome with dentinogenesis imperfecta
- Mandibulofacial dysostosis - macroblepharon - macrostomia
- Marcus-Gunn syndrome
- Marfan syndrome type 2
- Marfanoid habitus - inguinal hernia - advanced bone age
- Marfanoid habitus - intellectual disability, autosomal recessive
- Marfanoid syndrome, De Silva type
- Marinesco-Sjögren syndrome
- Maternal hyperphenylalaninemia
- Maxillonasal dysplasia
- Mayer-Rokitansky-Küster-Hauser syndrome
- Medeira-Dennis-Donnai syndrome
- Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
- Meige disease
- Mendelian susceptibility to mycobacterial diseases
- Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
- Mesomelic dwarfism - cleft palate - camptodactyly
- Metabolic disease associated with ocular features
- Metabolic disease due to other fatty acid oxidation disorder
- Metabolic disease with cataract
- Metabolic disease with corneal opacity
- Metabolic disease with dementia
