Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Rabson–Mendenhall_syndrome> ?p ?o }
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- Rabson–Mendenhall_syndrome abstract "Rabson–Mendenhall syndrome is a rare autosomal recessive disorder characterized by severe insulin resistance. The disorder is caused by mutations in the insulin receptor gene. Symptoms include growth abnormalities of the head, face and nails, along with the development of acanthosis nigricans. Treatment involves controlling blood glucose levels by using insulin and incorporating a strategically planned, controlled diet. Also, direct actions against other symptoms may be taken (e.g. surgery for facial abnormalities) This syndrome usually affects children and has a prognosis of 1–2 years.".
- Rabson–Mendenhall_syndrome icd10 "E13".
- Rabson–Mendenhall_syndrome omim "262190".
- Rabson–Mendenhall_syndrome wikiPageID "9920555".
- Rabson–Mendenhall_syndrome wikiPageLength "10293".
- Rabson–Mendenhall_syndrome wikiPageOutDegree "35".
- Rabson–Mendenhall_syndrome wikiPageRevisionID "677873995".
- Rabson–Mendenhall_syndrome wikiPageWikiLink Acanthosis_nigricans.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Autosomal_recessive.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Category:Autosomal_recessive_disorders.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Category:Rare_diseases.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Category:Syndromes.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Chromosome_19.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Chromosome_19_(human).
- Rabson–Mendenhall_syndrome wikiPageWikiLink Dentition.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Diabetes_mellitus_type_2.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Diabetic_ketoacidosis.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Dominance_(genetics).
- Rabson–Mendenhall_syndrome wikiPageWikiLink Donohue_syndrome.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Dysplasia.
- Rabson–Mendenhall_syndrome wikiPageWikiLink FPG.
- Rabson–Mendenhall_syndrome wikiPageWikiLink File:Autorecessive.svg.
- Rabson–Mendenhall_syndrome wikiPageWikiLink GTT.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Hirsutism.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Hyperglycemia.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Hyperinsulinemia.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Hyperkeratosis.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Hyperpigmentation.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Hyperplasia.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Hypoglycemia.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Insulin.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Insulin-like_growth_factor_1.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Insulin_receptor.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Ketoacidosis.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Leptin.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Metformin.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Ovarian_tumor.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Pioglitazone.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Precocious_puberty.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Prognathism.
- Rabson–Mendenhall_syndrome wikiPageWikiLink Wikt:facies.
- Rabson–Mendenhall_syndrome wikiPageWikiLinkText "Rabson–Mendenhall syndrome".
- Rabson–Mendenhall_syndrome hasPhotoCollection Rabson–Mendenhall_syndrome.
- Rabson–Mendenhall_syndrome icd "E13".
- Rabson–Mendenhall_syndrome name "Rabson–Mendenhall syndrome".
- Rabson–Mendenhall_syndrome omim "262190".
- Rabson–Mendenhall_syndrome wikiPageUsesTemplate Template:Cell_surface_receptor_deficiencies.
- Rabson–Mendenhall_syndrome wikiPageUsesTemplate Template:Endocrine_pathology.
- Rabson–Mendenhall_syndrome wikiPageUsesTemplate Template:Infobox_disease.
- Rabson–Mendenhall_syndrome wikiPageUsesTemplate Template:Reflist.
- Rabson–Mendenhall_syndrome subject Category:Autosomal_recessive_disorders.
- Rabson–Mendenhall_syndrome subject Category:Rare_diseases.
- Rabson–Mendenhall_syndrome subject Category:Syndromes.
- Rabson–Mendenhall_syndrome type Disease.
- Rabson–Mendenhall_syndrome type Thing.
- Rabson–Mendenhall_syndrome type Q12136.
- Rabson–Mendenhall_syndrome comment "Rabson–Mendenhall syndrome is a rare autosomal recessive disorder characterized by severe insulin resistance. The disorder is caused by mutations in the insulin receptor gene. Symptoms include growth abnormalities of the head, face and nails, along with the development of acanthosis nigricans. Treatment involves controlling blood glucose levels by using insulin and incorporating a strategically planned, controlled diet. Also, direct actions against other symptoms may be taken (e.g.".
- Rabson–Mendenhall_syndrome label "Rabson–Mendenhall syndrome".
- Rabson–Mendenhall_syndrome sameAs Sindrome_di_Rabson-Mendenhall.
- Rabson–Mendenhall_syndrome sameAs Zespół_Rabsona-Mendenhalla.
- Rabson–Mendenhall_syndrome sameAs m.02px1t_.
- Rabson–Mendenhall_syndrome sameAs Q3961685.
- Rabson–Mendenhall_syndrome sameAs Q3961685.
- Rabson–Mendenhall_syndrome wasDerivedFrom Rabson–Mendenhall_syndrome?oldid=677873995.
- Rabson–Mendenhall_syndrome isPrimaryTopicOf Rabson–Mendenhall_syndrome.
- Rabson–Mendenhall_syndrome name "Rabson–Mendenhall syndrome".