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Descriptor English: Osteoarthropathy, Primary Hypertrophic
Descriptor Spanish: Osteoartropatía Hipertrófica Primaria
Descriptor Portuguese: Osteoartropatia Hipertrófica Primária
Descriptor French: Pachydermopériostose
Entry term(s): Acropachies, Hereditary
Acropachy, Hereditary
Autosomal Dominant Pachydermoperiostoses
Autosomal Dominant Pachydermoperiostosis
Autosomal Recessive Pachydermoperiostosis
Clubbing of Digits
Cranioosteoarthropathies
Cranioosteoarthropathy
Currarino Idiopathic Osteoarthropathy
Digital Clubbing, Isolated Congenital
Familial Idiopathic Osteoarthropathy Of Childhood
Hereditary Acropachies
Hereditary Acropachy
Hypertrophic Osteoarthropathy, Idiopathic
Hypertrophic Osteoarthropathy, Primary
Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant
Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive
Idiopathic Hypertrophic Osteoarthropathy
Osteoarthropathy, Currarino Idiopathic
Osteoarthropathy, Idiopathic Hypertrophic
Pachydermoperiostoses, Autosomal Dominant
Pachydermoperiostosis
Pachydermoperiostosis, Autosomal Dominant
Pachydermoperiostosis, Autosomal Recessive
Primary Hypertrophic Osteoarthropathy
Primary Hypertrophic Osteoarthropathy, Autosomal Dominant
Recessive Pachydermoperiostosis, Autosomal
Touraine Solente Gole Syndrome
Touraine-Solente-Gole Syndrome
Tree number(s): C05.116.725
C05.550.648
C16.320.718
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D010004
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.
Annotation: OSTEOARTHROPATHY, SECONDARY HYPERTROPHIC is also available
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
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)
DeCS ID: 10180
Unique ID: D010004
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1965/01/01
Date of Entry: 1999/01/01
Revision Date: 2013/07/08
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.
Preferred term Osteoarthropathy, Primary Hypertrophic
Entry term(s) Autosomal Recessive Pachydermoperiostosis
Hypertrophic Osteoarthropathy, Idiopathic
Hypertrophic Osteoarthropathy, Primary
Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive
Idiopathic Hypertrophic Osteoarthropathy
Osteoarthropathy, Idiopathic Hypertrophic
Pachydermoperiostosis
Pachydermoperiostosis, Autosomal Recessive
Primary Hypertrophic Osteoarthropathy
Recessive Pachydermoperiostosis, Autosomal
Touraine Solente Gole Syndrome
Touraine-Solente-Gole Syndrome
Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant - Related but not broader or narrower
Concept UI M0567470
Preferred term Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant
Entry term(s) Autosomal Dominant Pachydermoperiostoses
Autosomal Dominant Pachydermoperiostosis
Pachydermoperiostoses, Autosomal Dominant
Pachydermoperiostosis, Autosomal Dominant
Primary Hypertrophic Osteoarthropathy, Autosomal Dominant
Cranioosteoarthropathy - Narrower
Concept UI M0567795
Preferred term Cranioosteoarthropathy
Entry term(s) Cranioosteoarthropathies
Currarino Idiopathic Osteoarthropathy
Familial Idiopathic Osteoarthropathy Of Childhood
Osteoarthropathy, Currarino Idiopathic
Digital Clubbing, Isolated Congenital - Related but not broader or narrower
Concept UI M0566418
Preferred term Digital Clubbing, Isolated Congenital
Entry term(s) Acropachies, Hereditary
Acropachy, Hereditary
Clubbing of Digits
Hereditary Acropachies
Hereditary Acropachy



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