Maffucci syndrome
Information
- Disease name
- Maffucci syndrome
- Disease ID
- DOID:0060221
- Description
- "A syndrome characterized by the presence of multiple enchondromas (benign growths of cartilage) associated with multiple hemangiomas." [url:http\://en.wikipedia.org/wiki/Maffucci_syndrome, url:http\://ghr.nlm.nih.gov/condition/maffucci-syndrome]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT04844697 | Completed | Resilience and Coping in a Rare Skeletal Disease Population to Face Coronavirus (COVID-19) Outbreak Distress: a Longitudinal Study | May 12, 2021 | December 31, 2022 | |
| NCT04134572 | Recruiting | Registry of Ollier Disease and Maffucci Syndrome | January 16, 2017 | January 2032 |
- Disase is a (Disease Ontology)
- DOID:225
- Cross Reference ID (Disease Ontology)
- GARD:6958
- Cross Reference ID (Disease Ontology)
- ICD10CM:Q78.4
- Cross Reference ID (Disease Ontology)
- MIM:614569
- Cross Reference ID (Disease Ontology)
- ORDO:163634
- OrphaNumber from OrphaNet (Orphanet)
- 163634