MeSH Browser

MeSH Heading: Osteoarthropathy, Primary Hypertrophic
Tree Number(s): C05.116.725; C05.550.648; C16.320.718
Unique ID: D010004
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D010004
Annotation: OSTEOARTHROPATHY, SECONDARY HYPERTROPHIC is also available
Scope Note: A condition chiefly characterized by thickening of the skin of the head and distal extremities, deep folds and furrows of the skin of the forehead, cheeks, and scalp, SEBORRHEA; HYPERHIDROSIS; periostosis of the long bones, digital clubbing, and spadelike enlargement of the hands and feet. It is more prevalent in the male, and is usually first evident during adolescence. Inheritance is primarily autosomal recessive, but an autosomal dominant form exists.
Entry Term(s): Acropachy, Hereditary; Clubbing of Digits; Cranioosteoarthropathy; Currarino Idiopathic Osteoarthropathy; Digital Clubbing, Isolated Congenital; Familial Idiopathic Osteoarthropathy Of Childhood; Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant; Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive; Idiopathic Hypertrophic Osteoarthropathy; Pachydermoperiostosis; Pachydermoperiostosis, Autosomal Dominant; Pachydermoperiostosis, Autosomal Recessive; Primary Hypertrophic Osteoarthropathy, Autosomal Dominant; Touraine-Solente-Gole Syndrome
Public MeSH Note: 2012; see OSTEOARTHROPATHY, PRIMARY HYPERTROPHIC 1964-2013; CRANIOOSTEOARTHROPATHY was indexed under OSTEOARTHROPATHY, PRIMARY HYPERTROPHIC 2012-2013; DIGITAL CLUBBING, ISOLATED CONGENITAL was indexed under NAILS, MALFORMED 2012-2013; HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL DOMINANT was indexed under OSTEOARTHROPATHY, PRIMARY HYPERTROPHIC 2012-2013
History Note: 2014(1964)
Date Established: 1965/01/01
Date of Entry: 1999/01/01
Revision Date: 2013/07/08

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)

Musculoskeletal Diseases [C05]
- Bone Diseases [C05.116]

Musculoskeletal Diseases [C05]
- Joint Diseases [C05.550]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]

Osteoarthropathy, Primary Hypertrophic Preferred

Concept UI: M0015511
Scope Note: A condition chiefly characterized by thickening of the skin of the head and distal extremities, deep folds and furrows of the skin of the forehead, cheeks, and scalp, SEBORRHEA; HYPERHIDROSIS; periostosis of the long bones, digital clubbing, and spadelike enlargement of the hands and feet. It is more prevalent in the male, and is usually first evident during adolescence. Inheritance is primarily autosomal recessive, but an autosomal dominant form exists.
Terms: Osteoarthropathy, Primary Hypertrophic Preferred Term
Term UI T029608
Date01/01/1999
LexicalTag NON
ThesaurusID; Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive
Term UI T811792
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Idiopathic Hypertrophic Osteoarthropathy
Term UI T769547
Date04/15/2010
LexicalTag NON
ThesaurusID; Pachydermoperiostosis
Term UI T029609
Date04/06/1984
LexicalTag NON
ThesaurusID; Pachydermoperiostosis, Autosomal Recessive
Term UI T811793
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Touraine-Solente-Gole Syndrome
Term UI T811790
Date11/15/2011
LexicalTag EPO
ThesaurusID OMIM (2013)

Digital Clubbing, Isolated Congenital Related

Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant Related

Cranioosteoarthropathy Narrower

Osteoarthropathy, Primary Hypertrophic MeSH Descriptor Data 2024