Experimental Factor Ontology
376 terms(s) returned
Term Type: | Record: 251 to 300 of 376 Records | Page: 6 of 8, First Previous Next Last | Show Records Per Page |
- lissencephaly type 1 due to doublecortin gene mutation
- lissencephaly type 3
- lissencephaly type 3-familial fetal akinesia sequence syndrome
- lissencephaly type 3-metacarpal bone dysplasia syndrome
- lissencephaly with cerebellar hypoplasia
- lissencephaly with cerebellar hypoplasia type A
- lissencephaly with cerebellar hypoplasia type B
- lissencephaly with cerebellar hypoplasia type C
- lissencephaly with cerebellar hypoplasia type D
- lissencephaly with cerebellar hypoplasia type E
- lissencephaly with cerebellar hypoplasia type F
- liver abscess (disease)
- liver adenosquamous carcinoma
- liver and intrahepatic bile duct neoplasm
- liver angiosarcoma
- liver cancer
- liver carcinoma in situ
- liver cavernous hemangioma
- liver disease, severe congenital
- liver extraskeletal osteosarcoma
- liver failure
- liver fibrosarcoma
- liver hemangioma
- liver inflammatory myofibroblastic tumor
- liver leiomyoma
- liver leiomyosarcoma
- liver lipoma
- liver lymphoma
- liver mesenchymal hamartoma
- liver neuroendocrine carcinoma
- liver rhabdomyosarcoma
- liver sarcoma
- liver solitary fibrous tumor
- lobar holoprosencephaly
- lobular neoplasia
- localized junctional epidermolysis bullosa, non-Herlitz type
- locational disease characteristic
- long COVID-19
- long QT syndrome 1
- long QT syndrome 10
- long QT syndrome 11
- long QT syndrome 12
- long QT syndrome 13
- long QT syndrome 14
- long QT syndrome 15
- long QT syndrome 16
- long QT syndrome 3
- long QT syndrome 5
- long QT syndrome 9
- long chain 3-hydroxyacyl-CoA dehydrogenase deficiency