| genetische passagère congenitale hypothyreoïdie (aandoening) | | genetische passagère congenitale hypothyreoïdie | | genetische voorbijgaande congenitale hypothyroïdie
| | Genetic transient congenital hypothyroidism | | Genetic transient congenital hypothyroidism is a rare, thyroid disease characterized by a gene mutation induced, temporary deficiency of thyroid hormones at birth, which later reverts to normal with or without replacement therapy in the first few months or years of life. |
| | Id | 770631009 | | 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 |
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| SNOMED CT to Orphanet simple map | 226316 |
| SNOMED CT to ICD-10 extended map | | Target | P72.2 | | Rule | TRUE | | Advice | ALWAYS P72.2 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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