skin neoplasm Maffucci syndrome https://rarediseases.info.nih.gov/diseases/6958/maffucci-syndrome https://www.malacards.org/card/multiple_enchondromatosis_maffucci_type enchondromatosis with multiple cavernous hemangiomas OMIM:614569 enchondromatosis with hemangiomata Dyschondrodysplasia with hemangiomas GARD:0006958 Kast syndrome Chondroplasia angiomatosis SCTID:46041001 Maffucci syndrome is a very rare genetic bone and skin disorder characterized by multiple enchondromas, leading to bone deformities, combined with multiple dark, irregularly shaped hemangiomas or less commonly lymphangiomas. multiple Angiomas and Endochondromas MONDO:0013808 Maffucci type enchondromatosis icd11.foundation:548780091 DOID:0060221 NCIT:C3213 chondrodysplasia with hemangioma Maffucci's anomalad Dyschondroplasia and cavernous hemangioma NORD:1393 Maffucci syndrome MEDGEN:7437 hemangiomata with Dyschondroplasia UMLS:C0024454 hemangiomatosis Chondrodystrophica Orphanet:163634 hereditary neoplastic syndrome skin vascular disease obsolete primary bone dysplasia with disorganized development of skeletal components overgrowth syndrome developmental defect during embryogenesis hereditary disorder of connective tissue vascular bone neoplasm hereditary skin disorder