Human Disease Ontology
401 terms(s) returned
| Term Type: | Record: 1 to 50 of 401 Records | Page: 1 of 9, First Previous Next Last | Show Records Per Page |
- L-2-hydroxyglutaric aciduria
- L-cell glucagon-like peptide producing tumor
- LADD syndrome
- La Crosse encephalitis
- Lafora disease
- Lambert-Eaton myasthenic syndrome
- Landau-Kleffner syndrome
- Langerhans cell sarcoma
- Langerhans-cell histiocytosis
- Laron syndrome
- Larsen syndrome
- Larsen-like syndrome B3GAT3 type
- Lassa fever
- Laurence-Moon syndrome
- Laurin-Sandrow 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 15
- Leber congenital amaurosis 16
- Leber congenital amaurosis 17
- 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
- Leber hereditary optic neuropathy and dystonia
- Leber hereditary optic neuropathy with demyelinating disease of CNS
- Leber plus disease
- Legg-Calve-Perthes disease
- Legionnaires' disease
- Legius syndrome
- Leigh disease
- Lemierre's syndrome
- Lennox-Gastaut syndrome
- Lenz-Majewski hyperostotic dwarfism
- Leri-Weill dyschondrosteosis
- Lesch-Nyhan syndrome
- Lewy body dementia
- Leydig cell hypoplasia
