Property:Has condition classification
From WikiMSK
This is a property of type Text.
C
Formative, resting, and resorptive stages. +
CESS (cauda equina suspected), CESI (cauda equina incomplete), CESR (cauda equina with urinary retention). +
Typical and atypical phenotypes +
Phenotypic spectrum ranging from severe Ullrich congenital muscular dystrophy (UCMD) with early-onset weakness and contractures, to milder Bethlem myopathy with later onset and slower progression. +
Non-cardiac musculoskeletal chest pain syndrome; distinguished from Tietze syndrome by absence of swelling. +
D
Niwayama and Utsinger, and Resnick for research purposes +
Nodules, cords, contractures +
F
CAM, Pincer, or mixed +
Can be primary or secondary to another pain condition. +
H
HNPP is classified under hereditary demyelinating neuropathies and distinct from other polyneuropathies due to its episodic nature. +
Primary and secondary +
I
Infantile, Juvenile, Adolescent, Adult. +
Belong to the trigeminal autonomic cephalalgias. +
Proximal and distal forms. +
Extra-articular hip impingement condition. +
P
Pompe disease presents in two forms: infantile-onset, characterized by hypertrophic cardiomyopathy and hypotonia, and late-onset, characterized by limb girdle and axial weakness and respiratory insufficiency in late disease. +
S
Type I: rigid thoracic hyperkyphosis
Type II: lumbar disease +
Length-dependent, non-length dependent, or mono-multiplex neuropathy types based on symptom distribution. +
T
Neurogenic (NTOS), Arterial (ATOS), Venous (VTOS) +
