Experimental Factor Ontology
926 terms(s) returned
| Term Type: | Record: 801 to 850 of 926 Records | Page: 17 of 19, First Previous Next Last | Show Records Per Page |
- muscular dystrophy-dystroglycanopathy
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12
- muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8
- muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15
- muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1
- muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14
- muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2
- muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3
- muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4
- muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8
- muscular dystrophy-dystroglycanopathy type B5
- muscular dystrophy-dystroglycanopathy type B6
- muscular dystrophy-dystroglycanopathy, type A
- muscular dystrophy-dystroglycanopathy, type B
- muscular dystrophy-dystroglycanopathy, type C
- muscular dystrophy-white matter spongiosis syndrome
- muscular hypertrophy-hepatomegaly-polyhydramnios syndrome
- muscular pseudohypertrophy-hypothyroidism syndrome
- musculoskeletal system benign neoplasm
- musculoskeletal system cancer
- myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive
- mycobacterial infectious disease
- mycosis fungoides and variants
- mycotic endocarditis
- mycotoxicosis
- myelocystocele
- myelodysplastic syndrome associated with isolated del(5q)
- myelodysplastic syndrome with multilineage dysplasia
- myelodysplastic/myeloproliferative disease
- myelofibrosis
- myeloid hemopathy
- myeloid leukemia
- myeloid neoplasm associated with FGFR1 rearrangement
- myeloid neoplasm associated with PDGFRB rearrangement
- myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2
- myelomeningocele
- myeloperoxidase deficiency
- myeloproliferative neoplasm, unclassifiable
