hyperostosis, cortical, congenital

Preferred Label : hyperostosis, cortical, congenital;

MeSH definition : A disease of young infants characterized by soft tissue swellings over the affected bones, fever, and irritability, and marked by periods of remission and exacerbation. (Dorland, 27th ed);

MeSH synonym : congenital cortical hyperostoses; hyperostoses, cortical congenital; hyperostoses, congenital cortical; cortical hyperostoses, congenital; caffey de toni silvermann syndrome; cortical hyperostoses, infantile; infantile cortical hyperostosis; hyperostosis, congenital cortical; cortical hyperostosis, infantile; hyperostoses, infantile cortical; hyperostosis, infantile cortical; infantile cortical hyperostoses; syndrome, caffey-de toni-silvermann; congenital hyperostosis, cortical; congenital hyperostoses, cortical; cortical congenital hyperostoses; cortical hyperostosis, congenital; congenital cortical hyperostosis; cortical congenital hyperostosis; caffey-de toni-silvermann syndrome; familial caffey's disease; caffey's disease, familial; disease, familial caffey's; familial caffey disease; familial caffeys disease; caffey disease; disease, caffey; familial infantile cortical hyperostosis; hyperostosis, cortical congenital;

MeSH annotation : cortical refers to cortex of bone; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES;

Wikipedia link : https://en.wikipedia.org/wiki/Infantile cortical hyperostoses;

Details

Origin ID

D006958;

UMLS CUI

C0020497;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [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)
- Infantile cortical hyperostoses [ICD-11 More detail]
- Other specified disorders of bone [ICD-10 Sub-category (who)]
- Other specified disorders of bone [ICD-10 Sub-category]
Currated CISMeF NLP mapping
- Caffey disease [DO Concept]
- Caffey disease [OMIM Phenotype]
- Caffey disease [Radlex concept]
- Caffey disease [ORDO Disease]
- Caffey's disease [MedDRA LLT]
- Congenital Cortical Hyperostosis [NCIt concept]
- Infantile Cortical Hyperostosis [NCIt concept]
- Infantile cortical hyperostosis [MedDRA Preferred Term]
- Infantile cortical hyperostosis [ICD-11 More detail]
- Infantile cortical hyperostosis [PASCAL descriptor]
- Infantile cortical hyperostosis (disorder) [SNOMED CT concept]
- congenital cortical hyperostosis [Disease (Nov.)]
- infantile cortical hyperostosis [SNOMED Notion]
DO Cross reference
- Caffey disease [DO Concept]
Manual NTBT mappings (CISMeF)
- Neonatal osteosclerotic dysplasia [ORDO Disease]
- Non-chondrodysplastic malformation syndrome affecting bones [ORDO Disease]
Record concept(s)
- hyperostosis, cortical, congenital [MeSH concept]
Related MeSH Supplementary Concept(s)
- Kenny-Caffey syndrome, type 1 [MeSH Supplementary Concept]
- Kenny-Caffey syndrome, type 2 [MeSH Supplementary Concept]
- prenatal cortical hyperostosis, lethal [MeSH Supplementary Concept]
- tumoral calcinosis, hyperphosphatemic, familial [MeSH Supplementary Concept]
- tumoral calcinosis, normophosphatemic, familial [MeSH Supplementary Concept]
- worth syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Caffey disease [OMIM Phenotype]
- Caffey disease [ORDO Disease]
- Caffey disease [Radlex concept]
- Caffey disease [DO Concept]
- Caffey's disease [MedDRA LLT]
- Congenital Cortical Hyperostosis [NCIt concept]
- Infantile Cortical Hyperostosis [NCIt concept]
- Infantile cortical hyperostosis [MedDRA Preferred Term]
- Infantile cortical hyperostosis [ICD-11 More detail]
- Infantile cortical hyperostosis [PASCAL descriptor]
- Infantile cortical hyperostosis (disorder) [SNOMED CT concept]
- congenital cortical hyperostosis [Disease (Nov.)]
- infantile cortical hyperostosis [SNOMED Notion]

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