| dbo:abstract |
عسر الألبومين وفرط ثيروكسين الدم العائلي (بالإنجليزية: Familial dysalbuminemic hyperthyroxinemia) هو نوع من فرط ثيروكسين الدم المرتبط بطفرات في مورثة ألبيومين المصل البشري. ابتكر المصطلح عام 1982. (ar) Familial dysalbuminemic hyperthyroxinemia is a type of hyperthyroxinemia associated with mutations in the human serum albumin gene. The term was introduced in 1982. (en) |
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32942 |
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dbr:Mutation dbc:Albumin_disorders dbr:Hyperthyroxinemia dbc:Thyroid_disease dbr:Human_serum_albumin |
| dbp:diseasesdb |
32942 (xsd:integer) |
| dbp:field |
endocrinology (en) |
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Familial dysalbuminemic hyperthyroxinemia (en) |
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dbt:Thyroid_disease dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Reflist dbt:Endocrine-disease-stub |
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dbc:Albumin_disorders dbc:Thyroid_disease |
| gold:hypernym |
dbr:Hyperthyroxinemia |
| rdf:type |
owl:Thing wikidata:Q12136 yago:Abstraction100002137 yago:Attribute100024264 yago:Condition113920835 yago:Disease114070360 yago:Disorder114052403 yago:IllHealth114052046 yago:Illness114061805 yago:PathologicalState114051917 yago:PhysicalCondition114034177 dbo:Disease yago:State100024720 yago:WikicatAlbuminDisorders umbel-rc:AilmentCondition |
| rdfs:comment |
عسر الألبومين وفرط ثيروكسين الدم العائلي (بالإنجليزية: Familial dysalbuminemic hyperthyroxinemia) هو نوع من فرط ثيروكسين الدم المرتبط بطفرات في مورثة ألبيومين المصل البشري. ابتكر المصطلح عام 1982. (ar) Familial dysalbuminemic hyperthyroxinemia is a type of hyperthyroxinemia associated with mutations in the human serum albumin gene. The term was introduced in 1982. (en) |
| rdfs:label |
عسر الألبومين وفرط ثيروكسين الدم العائلي (ar) Familial dysalbuminemic hyperthyroxinemia (en) |
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freebase:Familial dysalbuminemic hyperthyroxinemia yago-res:Familial dysalbuminemic hyperthyroxinemia wikidata:Familial dysalbuminemic hyperthyroxinemia dbpedia-ar:Familial dysalbuminemic hyperthyroxinemia https://global.dbpedia.org/id/4k5jo |
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Familial dysalbuminemic hyperthyroxinemia (en) |
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wikipedia-en:Familial_dysalbuminemic_hyperthyroxinemia |