| syndroom van gingivale fibromatose en progressieve doofheid (aandoening) | | syndroom van gingivale fibromatose en progressieve doofheid | | Gingival fibromatosis with progressive deafness syndrome | | Jones syndrome
| | A rare syndrome characterized by gingival fibromatosis associated with progressive sensorineural hearing loss. It has been described in two families (with at least 16 affected members spanning five generations in one of the families, and five affected members spanning three generations in the other family). It is transmitted as an autosomal dominant trait. |
| | Id | 722449007 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| SNOMED CT to Orphanet simple map | 2027 |
| SNOMED CT to ICD-10 extended map | | Target | H90.3 | | Rule | TRUE | | Advice | ALWAYS H90.3 | 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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