n
(pathology) myotonia of the limbs
n
(medicine) A congenital condition in which there is a lack of muscle development
n
(pathology) atrophy of muscles
v
(intransitive, pathology) To suffer from ankylosis.
n
(pathology) A reduction in the functionality of an organ caused by disease, injury or lack of use.
n
(pathology) Any disease that affects growth
n
(pathology) A form of muscular dystrophy of the muscles of the shoulder and pelvic girdle
n
(pathology) An X-linked recessive retinal degenerative disease
n
The three symptoms of Currarino syndrome.
n
(pathology) One of three mechanical syndromes in the McKenzie method proposed in 1981 by the New Zealand physical therapist Robin McKenzie.
n
(pathology) Any form of myositis including dermatomyositis and polymyositis
n
(pathology) fetal malformation during growth of the embryo
n
The formation of abnormal tissue
n
(pathology) A recessive form of muscular dystrophy
adj
(pathology) That causes eclampsia
adj
Alternative form of encephalitogenic [That can cause encephalitis.]
n
(pathology) inflammation of the endoneurium
n
(medicine, pathology) A condition characterised by chronic pain, stiffness, and tenderness of the muscles, tendons, and joints.
n
A complex of clinical features caused mainly by vascular dysregulation. Symptoms include cold hands and feet and low blood pressure.
n
(medicine) A set of clinical criteria used to diagnose Marfan syndrome.
n
(pathology) A focal malformation consisting of disorganized arrangement of tissue types.
n
(medicine) hemorrhage of the spinal cord.
n
(pathology) All the inflammation networks in an organism
n
(medicine) dysplastic gangliocytoma of the cerebellum
n
(medicine) Exaggerated physical and sexual development in a young person
n
(pathology) Any medical condition characterised by impaired movement
n
(medicine) Muscular dystrophy.
adj
Pertaining to myalgia.
n
(pathology) A disease of muscle characterised by infiltration of macrophages
n
(pathology) The imaging of myopathies
n
(surgery) The displacement of muscle fibres
n
The permanent shortening (reduction in length) of a muscle
n
The disruption of muscle tone
n
A decrease in muscle mass
n
(neurology, pathology) Inflammation of one or more nerves.
n
neuritis accompanied by inflammation of the related muscles
n
Inflammation of a nerve.
n
A severe form of nerve injury in which both the axon and its encapsulating connective tissue lose their continuity.
n
(medicine) A mitochondrial myopathy with a typical onset before 20 years of age.
n
(medicine) A form of arthritis that only affects a few joints
adj
Of or relating to panencephalitis.
n
(pathology) An inherited form of myoclonus
n
(pathology) Abnormal laxity of a joint
n
(medicine) Inflammation of the perineurium.
n
(medicine) pain in several muscles
n
(medicine) An inflammatory disease affecting multiple muscles
n
inflammation of multiple nerves; multiple neuritis
n
(medicine, rare) A disease that affects multiple organs or functions.
n
(medicine) inflammation of the roots of the nerves
n
(medicine) A radiculopathy affecting more than one spinal nerve root.
n
(pathology) Any prion-related disease
n
(pathology) radiculopathy combined with myelopathy
n
(pathology) inflammation of the roots of a nerve
n
(pathology) Any disease of the spinal nerve roots and spinal nerves.
n
(pathology) neuropathy of the radiculoplexus
n
(medicine) A developmental syndrome caused by a defect in the genes of the RAS/MAPK pathway.
n
(pathology) injury to muscles and tendons caused by continuous repetitive use of particular muscle groups, especially in one's arms and hands, for example by using a keyboard and/or mouse, playing a musical instrument or working on an assembly line
n
(rare) A person suffering from rheumatism
adj
(archaic, medicine) Of or pertaining to rheumatism; rheumatic.
adj
(pathology) That causes rheumatism
n
(pathology) Gradual loss of skeletal muscle due to aging, immobility, illness, or combinations thereof.
n
(pathology) A form of muscular dystrophy related to a selenoprotein
n
(medicine) A disorder in which a cyst or cavity forms within the spinal cord, possibly leading to stiffness or paralysis.
n
(pathology) The production and development of tendinopathies
n
(pathology) A form of muscular dystrophy associated with defects in the TTN gene
n
(pathology) An autosomal-dominant form of muscular dystrophy
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