| Behr syndrome (disorder) | | Behr syndrome | | Behr complicated familial optic atrophy OPA1 gene related Behr syndrome
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| | Id | 718221007 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | H35.5 | | Rule | TRUE | | Advice | ALWAYS H35.5 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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