| congenitale afwezigheid van helft van schildklier (aandoening) | | congenitale afwezigheid van helft van schildklier | | congenitale afwezigheid van helft van glandula thyroidea
congenitale afwezigheid van helft van thyroïd
| | Thyroid hemiagenesis | | Congenital absence of half of thyroid
Congenital hemiagenesis of thyroid
| | Thyroid hemiagenesis is a form of thyroid dysgenesis characterized by an absence of half of the thyroid gland that is usually asymptomatic but may result in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth. |
| | Id | 715734006 | | Status | Primitive |
| SNOMED CT to Orphanet simple map |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | E03.1 | | Term | Congenitale hypothyroïdie zonder struma |
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| SNOMED CT to ICD-10 extended map | | Target | E03.1 | | Rule | TRUE | | Advice | ALWAYS E03.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
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