| syndroom van Möbius-syndroom, axonale neuropathie, hypogonadotropisch hypogonadisme (aandoening) | | syndroom van Möbius-syndroom, axonale neuropathie, hypogonadotropisch hypogonadisme | | syndroom van syndroom van Möbius, axonale neuropathie, hypogonadotropisch hypogonadisme
syndroom van möbiussyndroom, axonale neuropathie, hypogonadotropisch hypogonadisme
| | Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | | A very rare syndrome with characteristics of the association of Mobius syndrome (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. All of the reported cases were sporadic. |
| | Id | 724174003 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q87.0 | | Term | Congenitale gestoorde-ontwikkelingssyndromen waarbij voornamelijk aangezicht is aangedaan |
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| SNOMED CT to Orphanet simple map | 2560 |
| SNOMED CT to ICD-10 extended map | | Target | Q87.0 | | Rule | TRUE | | Advice | ALWAYS Q87.0 | 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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