congenitale hypothyreoïdie door maternale inname van thyreostaticum (aandoening) | | congenitale hypothyreoïdie door maternale inname van thyreostaticum | | aangeboren hypothyroïdie door inname van thyreostaticum door moeder
| | Congenital hypothyroidism due to maternal intake of antithyroid drug | | A rare congenital hypothyroidism disorder with characteristics of transient primary fetal or neonatal hypothyroidism resulting from transplacental transfer of antithyroid drugs due to maternal intake. Patients may present fetal or neonatal goiter, hoarse cry, reduced tendon reflexes, feeding difficulty, constipation, prolonged jaundice and/or respiratory distress. Elevated levels of T4 and thyroid stimulating hormone usually normalize without treatment within 3 weeks of birth. |
| Id | 783177006 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | Target | P72.2 | Term | Overige voorbijgaande neonatale stoornissen van schildklierfunctie, niet elders geclassificeerd |
Target | P04.1 | Term | Gevolgen voor foetus en pasgeborene door overige medicatie van moeder |
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SNOMED CT to Orphanet simple map | 226313 |
SNOMED CT to ICD-10 extended map | Target | P72.2 | Rule | TRUE | Advice | ALWAYS P72.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | Correlation | SNOMED CT source code to target map code correlation not specified |
Target | P04.1 | Rule | TRUE | Advice | ALWAYS P04.1 | Correlation | SNOMED CT source code to target map code correlation not specified |
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