Orthopedics conditions, page 5 of 5
9 conditions on this page, alphabetically from Tenosynovitis to X-linked spondyloepimetaphyseal dysplasia. Each entry below describes the condition in full.
On this page
Tenosynovitis
An arthropathy that is characterized as an inflammation of the lining of the sheath that surrounds a tendon. Patients with tenosynovitis are cared for through our Orthopedics service line.
Also known as
- Inflammation of tendon sheath
Classification
Ontology identifier: DOID:970 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › arthropathy.
Specialty: Orthopedics
Broader conditions
Medical codes
- MeSH: D013717
- SNOMED CT: 240035004
Care at Weyland-Yutani Health System
Orthopedics specialists lead care for tenosynovitis. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about tenosynovitis? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Tibial muscular dystrophy
A distal myopathy that is characterized by autosomal dominant inheritance of late-onset muscular dystrophy beginning in the anterior compartment of the legs that has_material_basis_in heterozygous mutation in the gene encoding the giant skeletal muscle protein titin (TTN) on chromosome 2q31. This page summarizes how tibial muscular dystrophy is classified and the care available at Weyland-Yutani Health System.
Also known as
- distal titinopathy
- Finnish tibial muscular dystrophy
- Tardive tibial muscular dystrophy
- TMD
- Udd myopathy
- Udd type distal myopathy
Classification
Ontology identifier: DOID:0111078 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal dominant disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- MeSH: D049310
- OMIM: 600334
- SNOMED CT: 698846009
Care at Weyland-Yutani Health System
Care for tibial muscular dystrophy is coordinated through Orthopedics. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
Related articles
When to seek care
Seek a medical evaluation if you are concerned about tibial muscular dystrophy. Bring a list of current medications and any previous test results.
Reference links
Tietze's syndrome
A cartilage disease that is characterized by localized tenderness and non-suppurative swelling, typically associated with the 2nd or 3rd costal cartilages unilaterally caused by inflammation of one or more of the costal cartilages and that has symptom anterior chest pain. This page summarizes how Tietze's syndrome is classified and the care available at Weyland-Yutani Health System.
Also known as
- Costalchondritis
- Costochondral junction syndrome
- Costochondritis
- Slipping rib syndrome
- Tietze's disease
Classification
Ontology identifier: DOID:14021 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › cartilage disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: M94.0
- ICD-9-CM: 733.6
- MeSH: D013991
- SNOMED CT: 156848001
Care at Weyland-Yutani Health System
Treatment of Tietze's syndrome begins with an evaluation in Orthopedics. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
Related articles
When to seek care
If you or a family member may have Tietze's syndrome, contact your primary care provider or schedule a visit with Orthopedics.
Reference links
Vitamin D-dependent rickets
Overview. A bone development disease that is characterized by softening and weakening of the bones, hypocalcemia, high levels of parathyroid hormone and hypophosphatemia. Weyland-Yutani Health System offers diagnosis and ongoing care for vitamin D-dependent rickets.
Classification
Ontology identifier: DOID:0080883 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › bone development disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: E55.0
- ICD-9-CM: 268.0
- SNOMED CT: 68295002
Care at Weyland-Yutani Health System
Care for vitamin D-dependent rickets is coordinated through Orthopedics. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
When to seek care
Questions about vitamin D-dependent rickets? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Vogt-Koyanagi-Harada disease
An autoimmune disease that is caused by T helper cell mediated autoimmune attack of melanocytes resulting in inflammation of the inside of the eye, whitening of hair, skin pigment loss, and meningitis. Patients with Vogt-Koyanagi-Harada disease are cared for through our Orthopedics service line.
Also known as
- Harada's disease
- uveomeningoencephalitic syndrome
- Vogt-Koyanagi syndrome
Classification
Ontology identifier: DOID:12297 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › autoimmune disease of musculoskeletal system › autoimmune disease of skin and connective tissue.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: H20.82
- ICD-9-CM: 364.24
- MeSH: D014607
- SNOMED CT: 44923005
Care at Weyland-Yutani Health System
Treatment of Vogt-Koyanagi-Harada disease begins with an evaluation in Orthopedics. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about Vogt-Koyanagi-Harada disease? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Volkmann contracture
In clinical terms, Volkmann contracture is described as follows: A connective tissue disease that develops from prolonged ischemia and results in permanent necrosis, stiffening, and shortening of affected muscles.
Also known as
- Volkmann's ischemic contracture
Classification
Ontology identifier: DOID:5587 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: T79.6
- ICD-9-CM: 958.6
- MeSH: D054061
- SNOMED CT: 157667008
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, Volkmann contracture is managed by Orthopedics with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about Volkmann contracture. Bring a list of current medications and any previous test results.
Reference links
Weissenbacher-Zweymuller syndrome
An osteochondrodysplasia that results_in shortened long bones and distinct facial abnormalities. Patients with Weissenbacher-Zweymuller syndrome are cared for through our Orthopedics service line.
Also known as
- Piere-Robin syndrome
- Pierre Robin Malformation
Classification
Ontology identifier: DOID:4258 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › bone development disease › osteochondrodysplasia.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: Q87.0
- MeSH: D010855
- OMIM: 261800
- SNOMED CT: 156908005
Care at Weyland-Yutani Health System
Care for Weissenbacher-Zweymuller syndrome is coordinated through Orthopedics. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
Related articles
When to seek care
If you or a family member may have Weissenbacher-Zweymuller syndrome, contact your primary care provider or schedule a visit with Orthopedics.
Reference links
Worth syndrome
A hyperostosis that has_material_basis_in a mutation in the LRP5 gene which results_in increased bone density and bony structures located_in palate. This page summarizes how Worth syndrome is classified and the care available at Weyland-Yutani Health System.
Also known as
- autosomal dominant endosteal hyperostosis
- autosomal dominant osteosclerosis
- benign form of Worth hyperostosis corticalis generalisata with torus platinus
- Worth's syndrome
Classification
Ontology identifier: DOID:0080037 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal dominant disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- MeSH: C536748
- OMIM: 144750
- SNOMED CT: 254131007
Care at Weyland-Yutani Health System
Care for Worth syndrome is coordinated through Orthopedics. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about Worth syndrome. Bring a list of current medications and any previous test results.
Reference links
X-linked spondyloepimetaphyseal dysplasia
A spondyloepimetaphyseal dysplasia that has_material_basis_in hemizygous mutation in BGN on chromosome Xq28. This page summarizes how X-linked spondyloepimetaphyseal dysplasia is classified and the care available at Weyland-Yutani Health System.
Also known as
Classification
Ontology identifier: DOID:0112150 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › X-linked monogenic disease › X-linked recessive disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- MeSH: C564714
- OMIM: 300106
- SNOMED CT: 770603000
Care at Weyland-Yutani Health System
Orthopedics specialists lead care for X-linked spondyloepimetaphyseal dysplasia. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about X-linked spondyloepimetaphyseal dysplasia. Bring a list of current medications and any previous test results.
Reference links