Mondo Disease Ontology
830 terms(s) returned
Term Type: | Record: 51 to 100 of 830 Records | Page: 2 of 17, First Previous Next Last | Show Records Per Page |
- Leber congenital amaurosis 14
- Leber congenital amaurosis 15
- Leber congenital amaurosis 16
- Leber congenital amaurosis 17
- 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 congenital amaurosis, non-human animal
- Leber hereditary optic neuropathy
- Leber hereditary optic neuropathy, autosomal recessive
- Leber hereditary optic neuropathy, cattle
- Leber hereditary optic neuropathy, non-human animal
- Leber optic atrophy and dystonia
- Leber optic atrophy, susceptibility to
- Leber plus disease
- Leber-like hereditary optic neuropathy, autosomal recessive 1
- Leber-like hereditary optic neuropathy, autosomal recessive 2
- Legg-Calve-Perthes disease
- Legionnaires' disease
- Legius syndrome
- Leigh syndrome
- Leigh syndrome with cardiomyopathy
- Lelis syndrome
- Lemierre syndrome
- Lennox-Gastaut syndrome
- Lenz-Majewski hyperostotic dwarfism
- Leri pleonosteosis
- Leri-Weill dyschondrosteosis
- Leriche syndrome
- Lesch-Nyhan phenotype with normal HGPRT
- Lesch-Nyhan syndrome
- Lessel-Kreienkamp syndrome
- Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome
- Lewis-Sumner syndrome
- Lewy body dementia
- Leydig cell hypoplasia
- Leydig cell hypoplasia due to complete LH resistance
- Leydig cell hypoplasia due to partial LH resistance
- Leydig cell hypoplasia, type 1
- Leydig cell tumor
- Lhermitte-Duclos disease
- Li-Campeau syndrome
- Li-Fraumeni syndrome
- Li-Ghorbani-Weisz-Hubshman syndrome