MeSH Browser

MeSH Heading: Hyperostosis, Cortical, Congenital
Tree Number(s): C05.116.099.708.479; C05.116.540.400; C16.614.465
Unique ID: D006958
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D006958
Annotation: cortical refers to cortex of bone; do not use /‌congen & do not coord with INFANT, NEWBORN, DISEASES
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)
Entry Version: HYPEROSTOSIS CORTICAL CONGEN
Entry Term(s): Caffey Disease; Caffey-De Toni-Silvermann Syndrome; Congenital Hyperostosis, Cortical; Cortical Congenital Hyperostosis; Cortical Hyperostosis, Congenital; Familial Caffey's Disease; Familial Infantile Cortical Hyperostosis; Infantile Cortical Hyperostosis
NLM Classification #: WS 430
Public MeSH Note: 91; was HYPEROSTOSIS, CORTICAL CONGENITAL 1964-90
Online Note: use HYPEROSTOSIS, CORTICAL, CONGENITAL to search HYPEROSTOSIS, CORTICAL CONGENITAL 1966-90
History Note: 91; was HYPEROSTOSIS, CORTICAL CONGENITAL 1964-90
Date Established: 1964/01/01
Date of Entry: 1999/01/01
Revision Date: 2012/07/03

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

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)
Terms: Hyperostosis, Cortical, Congenital Preferred Term
Term UI T020903
Date01/01/1999
LexicalTag NON
ThesaurusID NLM (1964); Caffey-De Toni-Silvermann Syndrome
Term UI T020899
Date04/06/1984
LexicalTag EPO
ThesaurusID UNK (19XX); Congenital Hyperostosis, Cortical
Term UI T020900
Date03/30/1974
LexicalTag NON
ThesaurusID UNK (19XX); Cortical Congenital Hyperostosis
Term UI T020901
Date03/30/1974
LexicalTag NON
ThesaurusID UNK (19XX); Cortical Hyperostosis, Congenital
Term UI T020902
Date04/05/1990
LexicalTag NON
ThesaurusID NLM (1991); Infantile Cortical Hyperostosis
Term UI T020904
Date03/30/1974
LexicalTag NON
ThesaurusID; Caffey Disease
Term UI T781889
Date12/09/2010
LexicalTag EPO
ThesaurusID; Familial Infantile Cortical Hyperostosis
Term UI T781890
Date12/09/2010
LexicalTag NON
ThesaurusID; Familial Caffey's Disease
Term UI T781891
Date12/09/2010
LexicalTag EPO
ThesaurusID

Hyperostosis, Cortical, Congenital MeSH Descriptor Data 2024