MeSH Browser

MeSH Heading: Arthrogryposis
Tree Number(s): C05.550.150; C05.651.102; C05.660.077; C16.131.621.077
Unique ID: D001176
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D001176
Annotation: "persistent flexure or contracture of a joint"; do not use /‌congen & do not coord with INFANT, NEWBORN, DISEASES
Scope Note: Persistent flexure or contracture of a joint.
Entry Term(s): Amyoplasia Congenita; Arthrogryposis Multiplex Congenita; Arthrogryposis Multiplex Congenita (AMC); Arthromyodysplasia, Congenital; Congenital Arthromyodysplasia; Congenital Multiple Arthrogryposis; Fibrous Ankylosis of Multiple Joints; Guerin-Stern Syndrome; Guérin-Stern Syndrome; Myodystrophia Fetalis Deformans; Otto Syndrome; Rocher-Sheldon Syndrome; Rossi Syndrome
NLM Classification #: WE 304
Public MeSH Note: 65
History Note: 65(63)
Date Established: 1965/01/01
Date of Entry: 1999/01/01
Revision Date: 2018/11/02

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]
- Joint Diseases [C05.550]

Musculoskeletal Diseases [C05]
- Muscular Diseases [C05.651]

Musculoskeletal Diseases [C05]
- Musculoskeletal Abnormalities [C05.660]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
  - Musculoskeletal Abnormalities [C16.131.621]

Arthrogryposis Preferred

Concept UI: M0001754
Scope Note: Persistent flexure or contracture of a joint.
Terms: Arthrogryposis Preferred Term
Term UI T003516
Date01/01/1999
LexicalTag NON
ThesaurusID NLM (1963); Amyoplasia Congenita
Term UI T003515
Date01/01/1975
LexicalTag NON
ThesaurusID; Arthromyodysplasia, Congenital
Term UI T003518
Date03/29/1974
LexicalTag NON
ThesaurusID UNK (19XX); Congenital Arthromyodysplasia
Term UI T003517
Date03/29/1974
LexicalTag NON
ThesaurusID UNK (19XX); Guerin-Stern Syndrome
Term UI T003519
Date03/29/1974
LexicalTag EPO
ThesaurusID UNK (19XX); Myodystrophia Fetalis Deformans
Term UI T003520
Date03/29/1974
LexicalTag NON
ThesaurusID UNK (19XX); Arthrogryposis Multiplex Congenita (AMC)
Term UI T834237
Date12/12/2012
LexicalTag ABX
ThesaurusID ORD (2010); Congenital Multiple Arthrogryposis
Term UI T834238
Date12/12/2012
LexicalTag NON
ThesaurusID ORD (2010); Fibrous Ankylosis of Multiple Joints
Term UI T834239
Date12/12/2012
LexicalTag NON
ThesaurusID ORD (2010); Guérin-Stern Syndrome
Term UI T834240
Date12/12/2012
LexicalTag EPO
ThesaurusID ORD (2010); Otto Syndrome
Term UI T834241
Date12/12/2012
LexicalTag EPO
ThesaurusID ORD (2010); Rocher-Sheldon Syndrome
Term UI T834242
Date12/12/2012
LexicalTag EPO
ThesaurusID ORD (2010); Rossi Syndrome
Term UI T834243
Date12/12/2012
LexicalTag EPO
ThesaurusID ORD (2010); Arthrogryposis Multiplex Congenita
Term UI T834244
Date12/12/2012
LexicalTag NON
ThesaurusID ORD (2010)

Arthrogryposis MeSH Descriptor Data 2024