| Descriptor English: | Osteoarthropathy, Primary Hypertrophic | ||||||
| Descriptor Spanish: |
Osteoartropatía Hipertrófica Primaria
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| 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 |
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| Tree number(s): |
C05.116.725 C05.550.648 C16.320.718 |
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| 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. |
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| Annotation: | OSTEOARTHROPATHY, SECONDARY HYPERTROPHIC is also available |
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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: | 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 |
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| History Note: | 2014(1964) |
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| 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 |
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Osteoarthropathy, Primary Hypertrophic
- Preferred
Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant
- Related but not broader or narrower
Cranioosteoarthropathy
- Narrower
Digital Clubbing, Isolated Congenital
- Related but not broader or narrower
| 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 |
| 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 |
| Concept UI |
M0567795 |
| Preferred term | Cranioosteoarthropathy |
| Entry term(s) |
Cranioosteoarthropathies Currarino Idiopathic Osteoarthropathy Familial Idiopathic Osteoarthropathy Of Childhood Osteoarthropathy, Currarino Idiopathic |
| 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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