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- Niemann–Pick_disease abstract "Niemann–Pick disease (/niːmənˈpɪk/ nee-mən-PIK) refers to a group of inherited severe metabolic disorders that allow sphingomyelin to accumulate in lysosomes, which are organelles in animal cells. The severe form is fatal in toddlerhood; people with milder forms may live into their teens or young adulthood. This disease involves dysfunctional metabolism of sphingolipids, which are fats found in cell membranes, so it is a kind of sphingolipidosis. Sphingolipidoses, in turn, are included in the larger family of lysosomal storage diseases (LSDs).".
- Niemann–Pick_disease thumbnail Autorecessive.jpg?width=300.
- Niemann–Pick_disease wikiPageID "769389".
- Niemann–Pick_disease wikiPageRevisionID "595579883".
- Niemann–Pick_disease diseasesdb "9016".
- Niemann–Pick_disease emedicinesubj "derm".
- Niemann–Pick_disease emedicinetopic "699".
- Niemann–Pick_disease genereviewsname "Acid Sphingomyelinase Deficiency — includes: Niemann–Pick Disease Type A, B".
- Niemann–Pick_disease genereviewsname "Niemann-Pick Disease Type C".
- Niemann–Pick_disease genereviewsnbk "NBK1296".
- Niemann–Pick_disease genereviewsnbk "NBK1370".
- Niemann–Pick_disease icd "272.7".
- Niemann–Pick_disease icd "E75.2".
- Niemann–Pick_disease medlineplus "1207".
- Niemann–Pick_disease meshid "D009542".
- Niemann–Pick_disease name "Niemann–Pick disease".
- Niemann–Pick_disease omim "257200".
- Niemann–Pick_disease subject Category:Ashkenazi_Jews_topics.
- Niemann–Pick_disease subject Category:Autosomal_recessive_disorders.
- Niemann–Pick_disease subject Category:Lipid_storage_disorders.
- Niemann–Pick_disease subject Category:Neurodegenerative_disorders.
- Niemann–Pick_disease subject Category:Rare_diseases.
- Niemann–Pick_disease subject Category:Skin_conditions_resulting_from_errors_in_metabolism.
- Niemann–Pick_disease type Disease.
- Niemann–Pick_disease type Situation.
- Niemann–Pick_disease comment "Niemann–Pick disease (/niːmənˈpɪk/ nee-mən-PIK) refers to a group of inherited severe metabolic disorders that allow sphingomyelin to accumulate in lysosomes, which are organelles in animal cells. The severe form is fatal in toddlerhood; people with milder forms may live into their teens or young adulthood. This disease involves dysfunctional metabolism of sphingolipids, which are fats found in cell membranes, so it is a kind of sphingolipidosis.".
- Niemann–Pick_disease label "Choroba Niemanna-Picka".
- Niemann–Pick_disease label "Doença de Niemann-Pick".
- Niemann–Pick_disease label "Enfermedad de Niemann-Pick".
- Niemann–Pick_disease label "Malattia di Niemann-Pick".
- Niemann–Pick_disease label "Niemann-Pick-Krankheit".
- Niemann–Pick_disease label "Niemann–Pick disease".
- Niemann–Pick_disease label "Болезнь Ниманна — Пика".
- Niemann–Pick_disease label "尼曼匹克症".
- Niemann–Pick_disease sameAs Niemann%E2%80%93Pick_disease.
- Niemann–Pick_disease sameAs Niemann-Pick-Krankheit.
- Niemann–Pick_disease sameAs Enfermedad_de_Niemann-Pick.
- Niemann–Pick_disease sameAs Malattia_di_Niemann-Pick.
- Niemann–Pick_disease sameAs Choroba_Niemanna-Picka.
- Niemann–Pick_disease sameAs Doença_de_Niemann-Pick.
- Niemann–Pick_disease sameAs Q1419931.
- Niemann–Pick_disease sameAs Q1419931.
- Niemann–Pick_disease wasDerivedFrom Niemann–Pick_disease?oldid=595579883.
- Niemann–Pick_disease depiction Autorecessive.jpg.
