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- Aspartylglucosaminuria abstract "Aspartylglucosaminuria ( commonly referred to as AGU) is an inherited disease that is characterized by a decline in mental functioning, accompanied by an increase in skin bone and joint issues. This disease is caused by a defect in an enzyme known as aspartylglucosaminidase. This enzyme plays a significant role in our body because it aids in breaking down certain sugars ( for example oligosaccharides) that are attached to specific proteins ( for example: glycoproteins). Aspartylglucosaminuria itself is characterized as a lysosomal disease because it does deal with inadequate activity in an enzymes function. Aspartylglucosaminidase function is to break down glycoproteins. These proteins are most abundant in the tissues of the body and in the surfaces of major organs, such as: the liver, spleen, thyroid and nerves. When glycoproteins are unable to be broken down then it causes aspartylglucosaminidase to back up in the lysosomes along with other substances. This back up causes damage to the tissues and organs that is progressive.".
- Aspartylglucosaminuria wikiPageExternalLink www.hideandseek.org.
- Aspartylglucosaminuria wikiPageExternalLink www.mannosidosis.org.
- Aspartylglucosaminuria wikiPageID "6702067".
- Aspartylglucosaminuria wikiPageRevisionID "588419731".
- Aspartylglucosaminuria hasPhotoCollection Aspartylglucosaminuria.
- Aspartylglucosaminuria wordnet_type synset-disease-noun-1.
- Aspartylglucosaminuria subject Category:Autosomal_recessive_disorders.
- Aspartylglucosaminuria subject Category:Glycoprotein_metabolism_disorders.
- Aspartylglucosaminuria subject Category:Rare_diseases.
- Aspartylglucosaminuria type Abstraction100002137.
- Aspartylglucosaminuria type Attribute100024264.
- Aspartylglucosaminuria type AutosomalRecessiveDisorders.
- Aspartylglucosaminuria type Condition113920835.
- Aspartylglucosaminuria type Disease114070360.
- Aspartylglucosaminuria type Disorder114052403.
- Aspartylglucosaminuria type GlycoproteinMetabolismDisorders.
- Aspartylglucosaminuria type IllHealth114052046.
- Aspartylglucosaminuria type Illness114061805.
- Aspartylglucosaminuria type PathologicalState114051917.
- Aspartylglucosaminuria type PhysicalCondition114034177.
- Aspartylglucosaminuria type State100024720.
- Aspartylglucosaminuria type AilmentCondition.
- Aspartylglucosaminuria comment "Aspartylglucosaminuria ( commonly referred to as AGU) is an inherited disease that is characterized by a decline in mental functioning, accompanied by an increase in skin bone and joint issues. This disease is caused by a defect in an enzyme known as aspartylglucosaminidase. This enzyme plays a significant role in our body because it aids in breaking down certain sugars ( for example oligosaccharides) that are attached to specific proteins ( for example: glycoproteins).".
- Aspartylglucosaminuria label "Aspartilglucosaminuria".
- Aspartylglucosaminuria label "Aspartylglucosaminuria".
- Aspartylglucosaminuria label "Aspartyloglikozaminuria".
- Aspartylglucosaminuria sameAs Aspartilglucosaminuria.
- Aspartylglucosaminuria sameAs Aspartyloglikozaminuria.
- Aspartylglucosaminuria sameAs m.0gj2cq.
- Aspartylglucosaminuria sameAs Q4412533.
- Aspartylglucosaminuria sameAs Q4412533.
- Aspartylglucosaminuria sameAs 114.
- Aspartylglucosaminuria sameAs 1493.
- Aspartylglucosaminuria sameAs Aspartylglucosaminuria.
- Aspartylglucosaminuria wasDerivedFrom Aspartylglucosaminuria?oldid=588419731.
- Aspartylglucosaminuria isPrimaryTopicOf Aspartylglucosaminuria.