About: glycogen storage disease II

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: glycogen storage disease II Goto Sponge NotDistinct Permalink

An Entity of Type : http://wikiba.se/ontology#Item, within Data Space : wasabi.inria.fr associated with source document(s)

Attributes	Values
type	Item
label	glycogen storage disease II Enfermedad de Pompe Morbus Pompe Bolest skladištenja glikogena tipa II Choroba Pompego Penyakit Pompe Penyakit Pompe Pompe kasalligi Pompe xəstəliyi Pompeho choroba Pompen tauti Pompeova bolest doença de Pompe glycogeenstapelingsziekte type II glykogeninlagringssjukdom typ II maladie de Pompe malaltia de Pompe malattia di Pompe malsano de Pompe داء اختزان الغلايكوجين النمط الثاني Болезнь Помпе Захворювання Помпе Помпеова болест מחלת אגירת גליקוגן מסוג 2 گلیکوژنوز نوع دو ポンペ病庞贝氏症龐貝氏症龐貝氏症龐貝氏症
wdt:P279	metabolic disease neurological disorder nervous system disease cardiomyopathy rare disease lysosomal storage disease disposition occurrence quality overload disease phenomenon carbohydrate metabolism disease glycogen metabolism disorder intrinsic cardiomyopathy acquired metabolic disease disease of anatomical entity contributing factor disease of biological process heart disease health problem possibility temporal entity hereditary disorder state entity phenomenon nutritional and metabolic diseases genetic nervous system disorder genetic peripheral neuropathy rare genetic disease spatio-temporal entity carbohydrate metabolic disorder physiological condition condition propensity property muscular glycogenosis glycogen storage disease with hypertrophic cardiomyopathy lysosomal disease with hypertrophic cardiomyopathy lysosomal glycogen storage disease metabolic myopathy disease genetic disease muscular disease musculoskeletal disorder glycogen storage disease II restrictive cardiomyopathy phenotypic trait glycogen storage disease inherited metabolic disorder cardiovascular disease hypertrophic cardiomyopathy non-dystrophic myopathy peripheral neuropathy familial restrictive cardiomyopathy lysosomal disease with restrictive cardiomyopathy familial cardiomyopathy
wdt:P31	rare disease disposition occurrence quality phenomenon contributing factor health problem possibility temporal entity state entity phenomenon

Faceted Search & Find service v1.13.91 as of Mar 24 2020

Alternative Linked Data Documents: Sponger | ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3229 as of Jul 10 2020, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (94 GB total memory)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software