Arthrogryposis [artrogrypóza]
- Terms
-
amyoplasia congenita
arthrogryposis multiplex congenita
arthrogryposis universalis congenita
syndrom mnohočetných kloubních kontraktur
-
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
Persistent flexure or contracture of a joint.
- Annotation
- "persistent flexure or contracture of a joint"; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
- DUI
- D001176 MeSH Browser
- CUI
- M0001754
- History note
- 65(63)
- Public note
- 65
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 4
- CO
- complications 2
- DI
- diagnosis 12
- DG
- diagnostic imaging 1
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology 7
- GE
- genetics 10
- HI
- history
- IM
- immunology 1
- ME
- metabolism 1
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 2
- PP
- physiopathology 3
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation 3
- SU
- surgery 6
- TH
- therapy 5
- UR
- urine
- VE
- veterinary 1
- VI
- virology
Arthrogryposis and ectodermal dysplasia Disease MeSH Browser
Arthrogryposis epileptic seizures migrational brain disorder Disease MeSH Browser
Arthrogryposis multiplex congenita neurogenic type Disease MeSH Browser
Arthrogryposis multiplex congenita whistling face Disease MeSH Browser
Arthrogryposis multiplex congenita, distal type 1 Disease MeSH Browser
Arthrogryposis multiplex congenita, distal type 2 Disease MeSH Browser
Arthrogryposis multiplex congenita, distal, X-linked Disease MeSH Browser
Arthrogryposis multiplex with deafness, inguinal hernias, and early death Disease MeSH Browser
Arthrogryposis renal dysfunction cholestasis syndrome Disease MeSH Browser
Arthrogryposis, Distal, Type 10 Disease MeSH Browser
Arthrogryposis, Distal, Type 4 Disease MeSH Browser
Arthrogryposis, Distal, with Mental Retardation and Characteristic Facies Disease MeSH Browser
Arthrogryposis, X-Linked, Type V Disease MeSH Browser
Arthrogryposis, distal, type 2E Disease MeSH Browser
Arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies Disease MeSH Browser
Arthrogryposis-like hand anomaly and sensorineural deafness Disease MeSH Browser
Boylan Dew Greco syndrome Disease MeSH Browser
Bruck syndrome 1 Disease MeSH Browser
Bruck syndrome 2 Disease MeSH Browser
Camptodactyly-ichthyosis syndrome Disease MeSH Browser
Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome Disease MeSH Browser
Cerebrooculofacioskeletal Syndrome 2 Disease MeSH Browser
Cerebrooculofacioskeletal Syndrome 4 Disease MeSH Browser
Contractures ectodermal dysplasia cleft lip palate Disease MeSH Browser
Cyprus facial neuromusculoskeletal syndrome Disease MeSH Browser
Distal arthrogryposis Moore Weaver type Disease MeSH Browser
Distal arthrogryposis type 2B Disease MeSH Browser
German Syndrome Disease MeSH Browser
Gordon syndrome Disease MeSH Browser
Hecht syndrome Disease MeSH Browser
Holoprosencephaly with Fetal Akinesia-Hypokinesia Sequence Disease MeSH Browser
Jequier Kozlowski skeletal dysplasia Disease MeSH Browser
Johnston Aarons Schelley syndrome Disease MeSH Browser
Kuskokwim disease Disease MeSH Browser
Ladda Zonana Ramer syndrome Disease MeSH Browser
Lethal Arthrogryposis With Anterior Horn Cell Disease Disease MeSH Browser
Lethal Congenital Contracture Syndrome 2 Disease MeSH Browser
Lethal congenital contracture syndrome 1 Disease MeSH Browser
Massa Casaer Ceulemans syndrome Disease MeSH Browser
Minicore myopathy, antenatal onset, with arthrogryposis Disease MeSH Browser
Multiple Pterygium Syndrome, Autosomal Dominant Disease MeSH Browser
Muscular Dystrophy, Congenital, Producing Arthrogryposis Disease MeSH Browser
Neuropathy, congenital, with arthrogryposis multiplex Disease MeSH Browser
Oculomelic amyoplasia Disease MeSH Browser
Pelvic dysplasia arthrogryposis of lower limbs Disease MeSH Browser
Pena Shokeir syndrome, type 1 Disease MeSH Browser
Podder-Tolmie syndrome Disease MeSH Browser
Ray Peterson Scott syndrome Disease MeSH Browser
Spondylohypoplasia, arthrogryposis and popliteal pterygium Disease MeSH Browser
Spranger Schinzel Myers syndrome Disease MeSH Browser
Tomaculous neuropathy Disease MeSH Browser