arthrogryposis

Preferred Label : arthrogryposis;

MeSH definition : Persistent flexure or contracture of a joint. ; Persistent flexure or contracture of a joint.;

MeSH synonym : guerin-stern syndrome; amyoplasia congenita; arthromyodysplasia, congenital; myodystrophia fetalis deformans; congenital arthromyodysplasias; syndrome, guerin-stern; arthromyodysplasias, congenital; arthrogryposes; congenital arthromyodysplasia; guerin stern syndrome; arthrogryposis multiplex congenita (AMC); arthrogryposis multiplex congenitas (AMC); congenita, arthrogryposis multiplex (AMC); congenitas, arthrogryposis multiplex (AMC); multiplex congenita, arthrogryposis (AMC); multiplex congenitas, arthrogryposis (AMC); fibrous ankylosis of multiple joints; otto syndrome; syndrome, otto; Rocher-Sheldon syndrome; rocher sheldon syndrome; syndrome, Rocher-Sheldon; rossi syndrome; syndrome, rossi; arthrogryposis multiplex congenita; arthrogryposis multiplex congenitas; congenita, arthrogryposis multiplex; congenitas, arthrogryposis multiplex; multiplex congenita, arthrogryposis; multiplex congenitas, arthrogryposis; congenital multiple arthrogryposis; arthrogryposes, congenital multiple; arthrogryposis, congenital multiple; congenital multiple arthrogryposes; multiple arthrogryposes, congenital; multiple arthrogryposis, congenital; Guérin-Stern Syndrome; Guérin Stern Syndrome; Syndrome, Guérin-Stern;

DeCS synonym : Gu rin-Stern Syndrome; Gu rin Stern Syndrome;

MeSH annotation : persistent flexure or contracture of a joint; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES;

Wikipedia link : https://en.wikipedia.org/wiki/Arthrogryposis;

Details

Origin ID

D001176;

UMLS CUI

C5779613;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- ANION GAP ABNORMAL [WHO-ART Preferred Term]
- Alanylglutamine [NCIt concept]
- Amyoplasia congenita disruptive sequence (disorder) [SNOMED CT concept]
- Anion gap [LOINC component]
- Anion gap [MedDRA Preferred Term]
- Antigua and Barbuda [NCIt concept]
- Arthrogryposis multiplex congenita [ICD-10 Sub-category]
- Arthrogryposis multiplex congenita [ICD-11 Sub-sub category]
- Arthrogryposis multiplex congenita [ICD-10 Sub-category (who)]
- Arthrogryposis multiplex congenita [OMIM phenotypic series]
- Arthrogryposis multiplex congenita [ORDO Disease]
- Arthrogryposis multiplex congenita [OMIM Phenotype]
- Arthrogryposis multiplex congenita-whistling face syndrome [ORDO Disease]
- Atrophic gastritis (disorder) [SNOMED CT concept]
- Chronic atrophic gastritis of unknown aetiology [ICD-11 Sub-sub category]
- Congenital amyoplasia [ORDO Disease]
- Congenital multiplex arthrogryposis [MedDRA Preferred Term]
- Left atrium [FMA entity]
- Other specified disorders of muscle [ICD-10 Sub-category (who)]
- Procedure Agents Domain [NCIt concept]
- amyoplasia congenita disruptive sequence [SNOMED Notion]
- anion gap [SNOMED Notion]
- distal arthrogryposis [DO Concept]
Currated CISMeF NLP mapping
- Arthrogryposis [PASCAL descriptor]
- Arthrogryposis [NCIt concept]
- Arthrogryposis [HRDO Sign]
- Arthrogryposis (disorder) [SNOMED CT concept]
- Arthrogryposis syndrome [ORDO Disease]
- arthrogryposis [Disease (Nov.)]
- arthrogryposis [SNOMED Notion]
False automatic mappings
- Arthrogryposis multiplex congenita [HPO term]
Manual BTNT mappings - CISMeF
- Adducted thumbs-arthrogryposis syndrome, Christian type [ORDO Disease]
- Arthrogryposis due to muscular dystrophy [ORDO Disease]
- Arthrogryposis-anterior horn cell disease syndrome [ORDO Disease]
- Arthrogryposis-hyperkeratosis syndrome, lethal form [ORDO Disease]
- Arthrogryposis-renal dysfunction-cholestasis syndrome [ORDO Disease]
- Autosomal recessive multiple pterygium syndrome [ORDO Disease]
- CAMFAK syndrome [ORDO Disease]
- Crisponi syndrome [ORDO Disease]
- Distal arthrogryposis [ORDO Disease]
- Fetal akinesia deformation sequence [ORDO Disease]
- Hypomyelination neuropathy-arthrogryposis syndrome [ORDO Disease]
- Infantile-onset X-linked spinal muscular atrophy [ORDO Disease]
- Kuskokwim syndrome [ORDO Disease]
- Lethal multiple pterygium syndrome [ORDO Disease]
- Marden-Walker syndrome [ORDO Disease]
- Multiple pterygium syndrome, Aslan type [ORDO Disease]
- Multiple pterygium-malignant hyperthermia syndrome [ORDO Disease]
- Musculocontractural Ehlers-Danlos syndrome [ORDO Disease]
- Neurogenic arthrogryposis multiplex congenita [ORDO Disease]
- Pelvic dysplasia-arthrogryposis of lower limbs syndrome [ORDO Disease]
- Van den Ende-Gupta syndrome [ORDO Disease]
- X-linked lethal multiple pterygium syndrome [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Sucking/swallowing disorder associated with a neuromuscular disease [ORDO Disease]
- Syndrome or malformation associated with head and neck malformations [ORDO Disease]
- Syndrome with limb malformations as a major feature [ORDO Disease]
ORDO relation(s)
- Arthrogryposis syndrome [ORDO Disease]
Record concept(s)
- arthrogryposis [MeSH concept]
Related MeSH Supplementary Concept(s)
- Holoprosencephaly with Fetal Akinesia-Hypokinesia Sequence [MeSH Supplementary Concept]
- Podder-Tolmie syndrome [MeSH Supplementary Concept]
- arthrogryposis and ectodermal dysplasia [MeSH Supplementary Concept]
- arthrogryposis epileptic seizures migrational brain disorder [MeSH Supplementary Concept]
- arthrogryposis multiplex congenita neurogenic type [MeSH Supplementary Concept]
- arthrogryposis multiplex congenita whistling face [MeSH Supplementary Concept]
- arthrogryposis multiplex congenita, distal type 1 [MeSH Supplementary Concept]
- arthrogryposis multiplex congenita, distal type 2 [MeSH Supplementary Concept]
- arthrogryposis multiplex congenita, distal, X-linked [MeSH Supplementary Concept]
- arthrogryposis multiplex with deafness, inguinal hernias, and early death [MeSH Supplementary Concept]
- arthrogryposis renal dysfunction cholestasis syndrome [MeSH Supplementary Concept]
- arthrogryposis, X-Linked, type V [MeSH Supplementary Concept]
- arthrogryposis, distal, type 10 [MeSH Supplementary Concept]
- arthrogryposis, distal, type 2E [MeSH Supplementary Concept]
- arthrogryposis, distal, type 4 [MeSH Supplementary Concept]
- arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies [MeSH Supplementary Concept]
- arthrogryposis, distal, with mental retardation and characteristic facies [MeSH Supplementary Concept]
- arthrogryposis-like hand anomaly and sensorineural deafness [MeSH Supplementary Concept]
- boylan dew greco syndrome [MeSH Supplementary Concept]
- bruck syndrome 1 [MeSH Supplementary Concept]
- bruck syndrome 2 [MeSH Supplementary Concept]
- camptodactyly-ichthyosis syndrome [MeSH Supplementary Concept]
- cataract, microcephaly, arthrogryposis, kyphosis syndrome [MeSH Supplementary Concept]
- cerebrooculofacioskeletal syndrome 2 [MeSH Supplementary Concept]
- cerebrooculofacioskeletal syndrome 4 [MeSH Supplementary Concept]
- contractures ectodermal dysplasia cleft lip palate [MeSH Supplementary Concept]
- cyprus facial neuromusculoskeletal syndrome [MeSH Supplementary Concept]
- distal arthrogryposis moore weaver type [MeSH Supplementary Concept]
- distal arthrogryposis type 2B [MeSH Supplementary Concept]
- german syndrome [MeSH Supplementary Concept]
- gordon syndrome [MeSH Supplementary Concept]
- hecht syndrome [MeSH Supplementary Concept]
- jequier kozlowski skeletal dysplasia [MeSH Supplementary Concept]
- johnston aarons schelley syndrome [MeSH Supplementary Concept]
- kuskokwim disease [MeSH Supplementary Concept]
- ladda zonana ramer syndrome [MeSH Supplementary Concept]
- lethal arthrogryposis with anterior horn cell disease [MeSH Supplementary Concept]
- lethal congenital contracture syndrome 1 [MeSH Supplementary Concept]
- lethal congenital contracture syndrome 2 [MeSH Supplementary Concept]
- massa casaer ceulemans syndrome [MeSH Supplementary Concept]
- minicore myopathy, antenatal onset, with arthrogryposis [MeSH Supplementary Concept]
- multiple pterygium syndrome, autosomal dominant [MeSH Supplementary Concept]
- muscular dystrophy, congenital, producing arthrogryposis [MeSH Supplementary Concept]
- neuropathy, congenital, with arthrogryposis multiplex [MeSH Supplementary Concept]
- oculomelic amyoplasia [MeSH Supplementary Concept]
- pelvic dysplasia arthrogryposis of lower limbs [MeSH Supplementary Concept]
- pena shokeir syndrome, type 1 [MeSH Supplementary Concept]
- ray peterson scott syndrome [MeSH Supplementary Concept]
- spondylohypoplasia, arthrogryposis and popliteal pterygium [MeSH Supplementary Concept]
- spranger schinzel myers syndrome [MeSH Supplementary Concept]
- tomaculous neuropathy [MeSH Supplementary Concept]
SNOMED CT : Morphologiquement associé
- contracture [MeSH Descriptor]
See also
- receptor, erbb-3 [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Arthrogryposis [HRDO Sign]
- Arthrogryposis [PASCAL descriptor]
- Arthrogryposis [NCIt concept]
- Arthrogryposis (disorder) [SNOMED CT concept]
- Arthrogryposis multiplex congenita [OMIM Phenotype]
- Arthrogryposis multiplex congenita [ICD-10 Sub-category]
- Arthrogryposis multiplex congenita [HPO term]
- Arthrogryposis multiplex congenita [ICD-10 Sub-category (who)]
- Arthrogryposis multiplex congenita (disorder) [SNOMED CT concept]
- Arthrogryposis syndrome [ORDO Disease]
- Congenital multiplex arthrogryposis [MedDRA Preferred Term]
- arthrogryposis [SNOMED Notion]
- arthrogryposis [Disease (Nov.)]
Validated automatic mappings to BTNT
- Arthrogryposis multiplex congenita (disorder) [SNOMED CT concept]
- arthrogryposis multiplex congenita [Disease (Nov.)]
- arthrogryposis multiplex congenita [DO Concept]

Keyword's position in hierarchy(ies) :

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