| Descriptor English: | Hyperostosis, Cortical, Congenital | ||||||
| Descriptor Spanish: |
Hiperostosis Cortical Congénita
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| Descriptor Portuguese: | Hiperostose Cortical Congênita | ||||||
| Descriptor French: | Hyperostose corticale infantile | ||||||
| Entry term(s): |
Caffey De Toni Silvermann Syndrome Caffey Disease Caffey's Disease, Familial Caffey-De Toni-Silvermann Syndrome Congenital Cortical Hyperostoses Congenital Cortical Hyperostosis Congenital Hyperostoses, Cortical Congenital Hyperostosis, Cortical Cortical Congenital Hyperostoses Cortical Congenital Hyperostosis Cortical Hyperostoses, Congenital Cortical Hyperostoses, Infantile Cortical Hyperostosis, Congenital Cortical Hyperostosis, Infantile Disease, Caffey Disease, Familial Caffey's Familial Caffey Disease Familial Caffey's Disease Familial Caffeys Disease Familial Infantile Cortical Hyperostosis Hyperostoses, Congenital Cortical Hyperostoses, Cortical Congenital Hyperostoses, Infantile Cortical Hyperostosis, Congenital Cortical Hyperostosis, Cortical Congenital Hyperostosis, Infantile Cortical Infantile Cortical Hyperostoses Infantile Cortical Hyperostosis Syndrome, Caffey-De Toni-Silvermann |
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| Tree number(s): |
C05.116.099.708.479 C05.116.540.400 C16.614.465 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D006958 | ||||||
| Scope note: | 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) |
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| Annotation: | cortical refers to cortex of bone; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 91; was HYPEROSTOSIS, CORTICAL CONGENITAL 1964-90 |
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| Online Note: | use HYPEROSTOSIS, CORTICAL, CONGENITAL to search HYPEROSTOSIS, CORTICAL CONGENITAL 1966-90 |
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| History Note: | 91; was HYPEROSTOSIS, CORTICAL CONGENITAL 1964-90 |
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| Entry Version: | HYPEROSTOSIS CORTICAL CONGEN |
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| DeCS ID: | 29270 | ||||||
| Unique ID: | D006958 | ||||||
| NLM Classification: | WE 250 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1964/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2012/07/03 |
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Hyperostosis, Cortical, Congenital
- Preferred
| Concept UI |
M0010841 |
| Scope note | 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) |
| Preferred term | Hyperostosis, Cortical, Congenital |
| Entry term(s) |
Caffey De Toni Silvermann Syndrome Caffey Disease Caffey's Disease, Familial Caffey-De Toni-Silvermann Syndrome Congenital Cortical Hyperostoses Congenital Cortical Hyperostosis Congenital Hyperostoses, Cortical Congenital Hyperostosis, Cortical Cortical Congenital Hyperostoses Cortical Congenital Hyperostosis Cortical Hyperostoses, Congenital Cortical Hyperostoses, Infantile Cortical Hyperostosis, Congenital Cortical Hyperostosis, Infantile Disease, Caffey Disease, Familial Caffey's Familial Caffey Disease Familial Caffey's Disease Familial Caffeys Disease Familial Infantile Cortical Hyperostosis Hyperostoses, Congenital Cortical Hyperostoses, Cortical Congenital Hyperostoses, Infantile Cortical Hyperostosis, Congenital Cortical Hyperostosis, Cortical Congenital Hyperostosis, Infantile Cortical Infantile Cortical Hyperostoses Infantile Cortical Hyperostosis Syndrome, Caffey-De Toni-Silvermann |
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