Matches in DBpedia 2014 for { <http://dbpedia.org/resource/Neutral_lipid_storage_disease> ?p ?o. }
Showing items 1 to 39 of
39
with 100 items per page.
- Neutral_lipid_storage_disease abstract "Neutral lipid storage disease (also known as Chanarin–Dorfman syndrome) is an autosomal recessive disorder characterized by accumulation of triglycerides in the cytoplasm of leukocytes, muscle, liver, fibroblasts, and other tissues.It can be associated with CGI58.".
- Neutral_lipid_storage_disease diseasesdb "32708".
- Neutral_lipid_storage_disease omim "275630".
- Neutral_lipid_storage_disease thumbnail Chanarin-Dorfman_Syndrome_smear_2009-11-13.JPG?width=300.
- Neutral_lipid_storage_disease wikiPageID "20673108".
- Neutral_lipid_storage_disease wikiPageRevisionID "592632323".
- Neutral_lipid_storage_disease diseasesdb "32708".
- Neutral_lipid_storage_disease hasPhotoCollection Neutral_lipid_storage_disease.
- Neutral_lipid_storage_disease name "Neutral lipid storage disease".
- Neutral_lipid_storage_disease omim "275630".
- Neutral_lipid_storage_disease subject Category:Enzyme_defects.
- Neutral_lipid_storage_disease subject Category:Genodermatoses.
- Neutral_lipid_storage_disease type Abstraction100002137.
- Neutral_lipid_storage_disease type Attribute100024264.
- Neutral_lipid_storage_disease type Condition113920835.
- Neutral_lipid_storage_disease type Defect114464005.
- Neutral_lipid_storage_disease type Disease114070360.
- Neutral_lipid_storage_disease type EnzymeDefects.
- Neutral_lipid_storage_disease type IllHealth114052046.
- Neutral_lipid_storage_disease type Illness114061805.
- Neutral_lipid_storage_disease type Imperfection114462666.
- Neutral_lipid_storage_disease type PathologicalState114051917.
- Neutral_lipid_storage_disease type PhysicalCondition114034177.
- Neutral_lipid_storage_disease type State100024720.
- Neutral_lipid_storage_disease type Disease.
- Neutral_lipid_storage_disease type AilmentCondition.
- Neutral_lipid_storage_disease type Situation.
- Neutral_lipid_storage_disease comment "Neutral lipid storage disease (also known as Chanarin–Dorfman syndrome) is an autosomal recessive disorder characterized by accumulation of triglycerides in the cytoplasm of leukocytes, muscle, liver, fibroblasts, and other tissues.It can be associated with CGI58.".
- Neutral_lipid_storage_disease label "Neutral lipid storage disease".
- Neutral_lipid_storage_disease sameAs Dorfman-Chanarin-Syndrom.
- Neutral_lipid_storage_disease sameAs m.0521lk5.
- Neutral_lipid_storage_disease sameAs Q7003001.
- Neutral_lipid_storage_disease sameAs Q7003001.
- Neutral_lipid_storage_disease sameAs 216.
- Neutral_lipid_storage_disease sameAs Neutral_lipid_storage_disease.
- Neutral_lipid_storage_disease wasDerivedFrom Neutral_lipid_storage_disease?oldid=592632323.
- Neutral_lipid_storage_disease depiction Chanarin-Dorfman_Syndrome_smear_2009-11-13.JPG.
- Neutral_lipid_storage_disease isPrimaryTopicOf Neutral_lipid_storage_disease.
- Neutral_lipid_storage_disease name "Neutral lipid storage disease".
