enchondromatosis

Preferred Label : enchondromatosis;

MeSH definition : Benign growths of cartilage in the metaphyses of several bones.;

MeSH synonym : enchondromas, multiple; enchondroses, multiple; enchondrosis, multiple; multiple enchondrosis; enchondromatoses; olliers disease; multiple enchondroma; disease, ollier's; enchondroma, multiple; ollier's disease; ollier disease; disease, ollier; multiple enchondromas; multiple enchondroses; enchondromatosis, multiple;

MeSH hyponym : maffucci syndrome; Syndrome, Maffucci; Enchondromatosis with Multiple Cavernous Hemangiomas; Hemangiomatosis Chondrodystrophica; Kast Syndrome; Hemangiomata with Dyschondroplasia; Chondrodysplasia with Hemangioma; Chondroplasia Angiomatosis; Dyschondroplasia and Cavernous Hemangioma; Enchondromatosis with Hemangiomata; Dyschondrodysplasia with Hemangiomas; Multiple Angiomas and Endochondromas;

MeSH annotation : non-neoplastic; do not confuse X ref OLLIER'S DISEASE with Ollier's disease as Ollier-Klippel-Trenaunay disease ( KLIPPEL-TRENAUNAY DISEASE); non-neoplastic; do not confuse entry term OLLIER'S DISEASE with Ollier's disease as Ollier-Klippel-Trenaunay disease ( KLIPPEL-TRENAUNAY DISEASE);

Wikipedia link : https://en.wikipedia.org/wiki/Enchondromatosis;

Details

Origin ID

D004687;

UMLS CUI

C0014084;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Maffucci syndrome [ICD-11 More detail]
- Maffucci syndrome [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- Enchondromatosis [PASCAL descriptor]
- Enchondromatosis [ICD-10 Sub-category]
- Enchondromatosis [ICD-11 More detail]
- Enchondromatosis [ICD-10 Sub-category (who)]
- Enchondromatosis [MedDRA Preferred Term]
- Enchondromatosis [NCIt concept]
- Enchondromatosis (disorder) [SNOMED CT concept]
- Enchondromatosis, multiple, ollier type [OMIM Phenotype]
- Enchondroses [HRDO Sign]
- Maffucci Syndrome [NCIt concept]
- Maffucci syndrome [PASCAL descriptor]
- Maffucci syndrome [Radlex concept]
- Maffucci syndrome [ORDO Disease]
- Maffucci syndrome (disorder) [SNOMED CT concept]
- Multiple enchondromatosis [HPO term]
- Multiple enchondromatosis, maffucci type [OMIM Phenotype]
- Ollier disease [DO Concept]
- Ollier disease [MedDRA LLT]
- Ollier disease [ORDO Disease]
- enchondromatosis [Disease (Nov.)]
- enchondromatosis [Radlex concept]
- maffucci syndrome [SNOMED Notion]
DO Cross reference
- Ollier disease [DO Concept]
False UMLS correspondences (reviewed by CISMeF team)
- Multiple enchondromatosis [HPO term]
- maffucci syndrome [SNOMED Notion]
- osteochondromatosis syndrome [SNOMED Notion]
False automatic mappings
- osteochondromatosis syndrome [SNOMED Notion]
HPO term
- Multiple enchondromatosis [HPO term]
Manual NTBT mappings (CISMeF)
- Complex vascular malformation with associated anomalies [ORDO Disease]
- Genetic bone tumor [ORDO Disease]
- Genetic skin vascular disorder [ORDO Disease]
- Inherited cancer-predisposing syndrome [ORDO Disease]
- Malformation syndrome with hamartosis [ORDO Disease]
- Non-chondrodysplastic malformation syndrome affecting bones [ORDO Disease]
- Overgrowth syndrome [ORDO Disease]
- Primary bone dysplasia with disorganized development of skeletal components [ORDO Disease]
- Rare bone tumor [ORDO Disease]
- Skin vascular disease [ORDO Disease]
ORDO relation(s)
- Ollier disease [ORDO Disease]
Record concept(s)
- enchondromatosis [MeSH concept]
- maffucci syndrome [MeSH concept]
See also (suggested by CISMeF)
- chondroma [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Enchondromatosis [ICD-10 Sub-category]
- Enchondromatosis [ICD-10 Sub-category (who)]
- Enchondromatosis [MedDRA Preferred Term]
- Enchondromatosis [PASCAL descriptor]
- Enchondromatosis [ICD-11 More detail]
- Enchondromatosis [NCIt concept]
- Enchondromatosis (disorder) [SNOMED CT concept]
- Enchondromatosis, multiple, ollier type [OMIM Phenotype]
- Enchondroses [HRDO Sign]
- Ollier disease [ORDO Disease]
- Ollier disease [MedDRA LLT]
- enchondromatosis [Radlex concept]
- enchondromatosis [Disease (Nov.)]
Validated automatic mappings to BTNT
- Maffucci syndrome [DO Concept]

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