Mondo Disease Ontology
885 terms(s) returned
| Term Type: | Record: 1 to 50 of 885 Records | Page: 1 of 18, First Previous Next Last | Show Records Per Page |
- L-2-hydroxyglutaric aciduria
- L-2-hydroxyglutaricacidemia, dog
- L-2-hydroxyglutaricacidemia, domestic cat
- L-2-hydroxyglutaricacidemia, non-human animal
- L-cell glucagon-like peptide-producing neuroendocrine tumor
- 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
- LRIT3-related retinopathy
- LRP5-related exudative vitreoretinopathy
- LRP5-related primary osteoporosis
- LTBP2-related ocular dysgenesis
- LZTFL1-related ciliopathy
- LZTR1-related schwannomatosis
- Lafora disease
- Lamb-Shaffer syndrome
- Lambert syndrome
- Lambert-Eaton myasthenic syndrome
- Lambotte syndrome
- Landau-Kleffner syndrome
- Landy-Donnai syndrome
- Lane Hamilton syndrome
- Langer mesomelic dysplasia
- Langerhans cell histiocytosis
- Langerhans cell histiocytosis specific to adulthood
- Langerhans cell histiocytosis specific to childhood
- Langerhans cell sarcoma
- Laron dwarfism, cattle
- Laron dwarfism, non-human animal
- Laron dwarfism, pig
- Laron syndrome
- Larsen syndrome
- Larsen-like osseous dysplasia-short stature syndrome
- Larsen-like syndrome, B3GAT3 type
- Lassa fever
- Laubry-Pezzi syndrome
- Laugier-Hunziker syndrome
- Laurence-Moon syndrome
- Laurence-Prosser-Rocker syndrome
