Human Disease Ontology
19651 terms(s) returned
| Term Type: | Record: 2001 to 2050 of 19651 Records | Page: 41 of 394, First Previous Next Last | Show Records Per Page |
- 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
- Legionella
- Legionella pneumophila
- Legionellaceae
- Legionellales
- Legionnaires' disease
- Legius syndrome
- Leigh disease
- Leishmania <genus>
- Leishmaniinae
- Lemierre's syndrome
- Lennox-Gastaut syndrome
- Lentivirus
- Lentivirus humimdef1
- Lentivirus humimdef2
- Lenz-Majewski hyperostotic dwarfism
- Leptospira
- Leptospiraceae
- Leptospirales
- Leptospiria
- Leptotrichiaceae
- Leptotrombidium
- Leptotrombidium deliense
- Leri-Weill dyschondrosteosis
- Lesch-Nyhan syndrome
- Lewy body dementia
- Leydig cell hypoplasia
- Leydig cell hypoplasia type I
- Leydig cell hypoplasia type II
- Leydig cell tumor
