Experimental Factor Ontology
375 terms(s) returned
| Term Type: | Record: 1 to 50 of 375 Records | Page: 1 of 8, 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
- LAMB2-related infantile-onset nephrotic syndrome
- LCAT deficiency
- LIPE-related familial partial lipodystrophy
- LMNA-related cardiocutaneous progeria syndrome
- LRP5-related exudative vitreoretinopathy
- LRP5-related primary osteoporosis
- LTBP2-related ocular dysgenesis
- Lafora disease
- 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 16
- Leber congenital amaurosis 17
- Leber congenital amaurosis 2
- Leber congenital amaurosis 8
- Leber congenital amaurosis 9
- Leber congenital amaurosis with early-onset deafness
- Leber hereditary optic neuropathy
- Leber hereditary optic neuropathy, autosomal recessive
- Leber plus disease
- Leber-like hereditary optic neuropathy, autosomal recessive 2
- Legg-Calve-Perthes disease
- Legius syndrome
- Leigh syndrome
- Leigh syndrome with cardiomyopathy
- Lelis syndrome
- Lennox-Gastaut syndrome
- Lenz-Majewski hyperostotic dwarfism
- Leri pleonosteosis
- Leri-Weill dyschondrosteosis
- Lesch-Nyhan syndrome
- Lessel-Kreienkamp syndrome
- Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome
- Leydig cell hypoplasia
- Leydig cell hypoplasia due to complete LH resistance
- Leydig cell hypoplasia due to partial LH resistance
