| syndroom van ectrodactylie van voet en centrale polydactylie (aandoening) | | syndroom van ectrodactylie van voet en centrale polydactylie | | SFMMP-syndroom
syndroom van gespleten voet en mesoaxiale polydactylie
| | Split-foot malformation, mesoaxial polydactyly syndrome | | SFMMP (split-foot malformation, mesoaxial polydactyly) syndrome
Split-foot malformation, mesoaxial polydactyly, nail abnormalities, sensorineural hearing loss syndrome
| | A rare genetic syndrome with limb malformations as a major feature with characteristics of unilateral or bilateral split-foot malformation, nail abnormalities of the hand and bilateral sensorineural hearing impairment. Mesoaxial polydactyly of the foot has also been described. |
| | Id | 1172635005 | | Status | Primitive |
| SNOMED CT to Orphanet simple map | 488232 |
| SNOMED CT to ICD-10 extended map | | Target | Q74.8 | | Rule | TRUE | | Advice | ALWAYS Q74.8 | 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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