Универсальный англо-русский словарь. Академик.ру. 2011.
ceroid-lipofuscinosis — neuronal ceroid lipofuscinosis a term for several genetic lipidoses of diverse biochemical and clinical characteristics, all characterized by progressive neurodegeneration, loss of vision, and a fatal course; the infantile type is Haltia… … Medical dictionary
Neuronal ceroid lipofuscinosis — Classification and external resources ICD 10 E75.4 ICD 9 330.1 … Wikipedia
lipofuscinosis — Abnormal storage of any one of a group of fatty pigments. ceroid l. SYN: Batten disease. neuronal ceroid l. a group of diseases characterized by accumulation of abnormal pigments in tissue (previously classified as … Medical dictionary
Infantile neuronal ceroid lipfuscinosis — Infobox Disease Name = Infantile neuronal ceroid lipfuscinosis Caption = DiseasesDB = 31533 ICD10 = ICD9 = ICDO = OMIM = 256730 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D009472 INCL, also known as Infantile Neuronal Ceroid… … Wikipedia
CLN — ceroid lipofuscinosis … Medical dictionary
CLN — • ceroid lipofuscinosis … Dictionary of medical acronyms & abbreviations
CLN5 — Ceroid lipofuscinosis, neuronal 5, also known as CLN5, is a human gene.cite web | title = Entrez Gene: CLN5 ceroid lipofuscinosis, neuronal 5| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=1203| accessdate … Wikipedia
CLN6 — Ceroid lipofuscinosis, neuronal 6, late infantile, variant, also known as CLN6, is a human gene.cite web | title = Entrez Gene: CLN6 ceroid lipofuscinosis, neuronal 6, late infantile, variant| url =… … Wikipedia
CLN3 — Ceroid lipofuscinosis, neuronal 3 Identifiers Symbols CLN3; BTS; JNCL; MGC102840 External IDs … Wikipedia
CLN8 — Ceroid lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation), also known as CLN8, is a human gene.cite web | title = Entrez Gene: CLN8 ceroid lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)| url =… … Wikipedia
Lysosomale Speicherkrankheiten — (LSK) sind eine Gruppe von etwa 45 genetisch bedingten Stoffwechselerkrankungen, die durch Fehlfunktionen im Lysosom ausgelöst werden. Die Erkrankungen sind monogenetisch.[1] In der angelsächsischen Fachliteratur wird meist der Begriff Lysosomal… … Deutsch Wikipedia
