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- Hartnup_disease abstract "Hartnup disease (also known as "pellagra-like dermatosis" and "Hartnup disorder") is an autosomal recessive metabolic disorder affecting the absorption of nonpolar amino acids (particularly tryptophan that can be, in turn, converted into serotonin, melatonin and niacin). Niacin is a precursor to nicotinamide, a necessary component of NAD+.The causative gene, SLC6A19, is located on chromosome 5.".
- Hartnup_disease diseasesdb "5638".
- Hartnup_disease emedicineSubject "derm".
- Hartnup_disease emedicineTopic "713".
- Hartnup_disease icd10 "E72.0".
- Hartnup_disease icd9 "270.0".
- Hartnup_disease medlineplus "001201".
- Hartnup_disease meshId "D006250".
- Hartnup_disease omim "234500".
- Hartnup_disease thumbnail L-tryptophan-skeletal.png?width=300.
- Hartnup_disease wikiPageExternalLink 001201.htm.
- Hartnup_disease wikiPageID "2441688".
- Hartnup_disease wikiPageRevisionID "592755515".
- Hartnup_disease caption Tryptophan.
- Hartnup_disease diseasesdb "5638".
- Hartnup_disease emedicinesubj "derm".
- Hartnup_disease emedicinetopic "713".
- Hartnup_disease hasPhotoCollection Hartnup_disease.
- Hartnup_disease icd "270".
- Hartnup_disease icd "E72.0".
- Hartnup_disease medlineplus "1201".
- Hartnup_disease meshid "D006250".
- Hartnup_disease name "Hartnup disease".
- Hartnup_disease omim "234500".
- Hartnup_disease wordnet_type synset-disease-noun-1.
- Hartnup_disease subject Category:Amino_acid_metabolism_disorders.
- Hartnup_disease subject Category:Autosomal_recessive_disorders.
- Hartnup_disease subject Category:Membrane_transport_protein_disorders.
- Hartnup_disease subject Category:Rare_diseases.
- Hartnup_disease subject Category:Skin_conditions_resulting_from_errors_in_metabolism.
- Hartnup_disease type Abstraction100002137.
- Hartnup_disease type AminoAcidMetabolismDisorders.
- Hartnup_disease type Attribute100024264.
- Hartnup_disease type AutosomalRecessiveDisorders.
- Hartnup_disease type Condition113920835.
- Hartnup_disease type Disorder114052403.
- Hartnup_disease type MembraneTransportProteinDisorders.
- Hartnup_disease type PhysicalCondition114034177.
- Hartnup_disease type SkinConditionsResultingFromErrorsInMetabolism.
- Hartnup_disease type State100024720.
- Hartnup_disease type Disease.
- Hartnup_disease type AilmentCondition.
- Hartnup_disease type Situation.
- Hartnup_disease comment "Hartnup disease (also known as "pellagra-like dermatosis" and "Hartnup disorder") is an autosomal recessive metabolic disorder affecting the absorption of nonpolar amino acids (particularly tryptophan that can be, in turn, converted into serotonin, melatonin and niacin). Niacin is a precursor to nicotinamide, a necessary component of NAD+.The causative gene, SLC6A19, is located on chromosome 5.".
- Hartnup_disease label "Choroba Hartnupów".
- Hartnup_disease label "Enfermedad de Hartnup".
- Hartnup_disease label "Hartnup disease".
- Hartnup_disease label "Hartnup-Krankheit".
- Hartnup_disease label "Maladie de Hartnup".
- Hartnup_disease label "Malattia di Hartnup".
- Hartnup_disease label "Ziekte van Hartnup".
- Hartnup_disease sameAs Hartnup-Krankheit.
- Hartnup_disease sameAs Enfermedad_de_Hartnup.
- Hartnup_disease sameAs Maladie_de_Hartnup.
- Hartnup_disease sameAs Malattia_di_Hartnup.
- Hartnup_disease sameAs Ziekte_van_Hartnup.
- Hartnup_disease sameAs Choroba_Hartnupów.
- Hartnup_disease sameAs m.07d8_j.
- Hartnup_disease sameAs Q200985.
- Hartnup_disease sameAs Q200985.
- Hartnup_disease sameAs Hartnup_disease.
- Hartnup_disease wasDerivedFrom Hartnup_disease?oldid=592755515.
- Hartnup_disease depiction L-tryptophan-skeletal.png.
- Hartnup_disease isPrimaryTopicOf Hartnup_disease.
- Hartnup_disease name "Hartnup disease".
