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- Hypertryptophanemia abstract "Hypertryptophanemia, also called familial hypertryptophanemia, is a rare autosomal recessive metabolic disorder that results in a massive buildup of the amino acid tryptophan in the blood, with associated symptoms and tryptophanuria (-uria denotes "in the urine").Elevated levels of tryptophan are also seen in Hartnup disease, a disorder of amino acid transport. However, the increase of tryptophan in that disorder is negligible when compared to that of hypertryptophanemia.".
- Hypertryptophanemia icd10 "E70.8".
- Hypertryptophanemia icd9 "270.2".
- Hypertryptophanemia omim "600627".
- Hypertryptophanemia thumbnail L-tryptophan-skeletal.png?width=300.
- Hypertryptophanemia wikiPageID "20271570".
- Hypertryptophanemia wikiPageRevisionID "597452780".
- Hypertryptophanemia caption Tryptophan.
- Hypertryptophanemia hasPhotoCollection Hypertryptophanemia.
- Hypertryptophanemia icd "270.2".
- Hypertryptophanemia icd "E70.8".
- Hypertryptophanemia name "Hypertryptophanemia".
- Hypertryptophanemia omim "600627".
- Hypertryptophanemia subject Category:Amino_acid_metabolism_disorders.
- Hypertryptophanemia subject Category:Autosomal_recessive_disorders.
- Hypertryptophanemia subject Category:Rare_diseases.
- Hypertryptophanemia type Abstraction100002137.
- Hypertryptophanemia type AminoAcidMetabolismDisorders.
- Hypertryptophanemia type Attribute100024264.
- Hypertryptophanemia type AutosomalRecessiveDisorders.
- Hypertryptophanemia type Condition113920835.
- Hypertryptophanemia type Disease114070360.
- Hypertryptophanemia type Disorder114052403.
- Hypertryptophanemia type IllHealth114052046.
- Hypertryptophanemia type Illness114061805.
- Hypertryptophanemia type PathologicalState114051917.
- Hypertryptophanemia type PhysicalCondition114034177.
- Hypertryptophanemia type State100024720.
- Hypertryptophanemia type Disease.
- Hypertryptophanemia type AilmentCondition.
- Hypertryptophanemia type Situation.
- Hypertryptophanemia comment "Hypertryptophanemia, also called familial hypertryptophanemia, is a rare autosomal recessive metabolic disorder that results in a massive buildup of the amino acid tryptophan in the blood, with associated symptoms and tryptophanuria (-uria denotes "in the urine").Elevated levels of tryptophan are also seen in Hartnup disease, a disorder of amino acid transport. However, the increase of tryptophan in that disorder is negligible when compared to that of hypertryptophanemia.".
- Hypertryptophanemia label "Hypertryptophanemia".
- Hypertryptophanemia sameAs m.04zwqt1.
- Hypertryptophanemia sameAs Q5958803.
- Hypertryptophanemia sameAs Q5958803.
- Hypertryptophanemia sameAs Hypertryptophanemia.
- Hypertryptophanemia wasDerivedFrom Hypertryptophanemia?oldid=597452780.
- Hypertryptophanemia depiction L-tryptophan-skeletal.png.
- Hypertryptophanemia isPrimaryTopicOf Hypertryptophanemia.
- Hypertryptophanemia name "Hypertryptophanemia".
