Experimental Factor Ontology
445 terms(s) returned
| Term Type: | Record: 1 to 50 of 445 Records | Page: 1 of 9, First Previous Next Last | Show Records Per Page |
- L-2-hydroxyglutaric aciduria
- L-ferritin deficiency
- L1 syndrome
- LADD syndrome
- LADD syndrome 1
- LAMA2-related muscular dystrophy
- LAMA5-related multisystemic syndrome
- LAMB2-related infantile-onset nephrotic syndrome
- LCA5-related retinopathy
- LCAT deficiency
- LEOPARD syndrome 1
- LEOPARD syndrome 2
- LEOPARD syndrome 3
- LIPE-related familial partial lipodystrophy
- LMNA-related cardiocutaneous progeria syndrome
- LRP5-related exudative vitreoretinopathy
- LRP5-related primary osteoporosis
- LTBP2-related ocular dysgenesis
- LZTR1-related schwannomatosis
- Lafora disease
- Lamb-Shaffer syndrome
- Lambert syndrome
- Langer mesomelic dysplasia
- Laron syndrome
- Larsen syndrome
- Larsen-like osseous dysplasia-short stature syndrome
- Larsen-like syndrome, B3GAT3 type
- Laubry-Pezzi syndrome
- Laurence-Moon syndrome
- Leber congenital amaurosis
- Leber congenital amaurosis 1
- Leber congenital amaurosis 10
- Leber congenital amaurosis 11
- Leber congenital amaurosis 12
- Leber congenital amaurosis 13
- Leber congenital amaurosis 14
- Leber congenital amaurosis 16
- Leber congenital amaurosis 17
- Leber congenital amaurosis 18
- Leber congenital amaurosis 19
- Leber congenital amaurosis 2
- Leber congenital amaurosis 3
- Leber congenital amaurosis 4
- Leber congenital amaurosis 5
- Leber congenital amaurosis 6
- Leber congenital amaurosis 7
- Leber congenital amaurosis 8
- Leber congenital amaurosis 9
- Leber congenital amaurosis with early-onset deafness
- Leber hereditary optic neuropathy
