Orthopedics conditions, page 4 of 5
20 conditions on this page, alphabetically from Panniculitis to Synpolydactyly. Each entry below describes the condition in full.
On this page
Panniculitis
A skin disease that is characterized by inflammation of subcutaneous adipose tissue. This page summarizes how panniculitis is classified and the care available at Weyland-Yutani Health System.
Classification
Ontology identifier: DOID:1526 (Human Disease Ontology).
Classification path: disease of anatomical entity › integumentary system disease › skin disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: M79.3
- ICD-9-CM: 729.30
- MeSH: D015434
- SNOMED CT: 268122002
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, panniculitis is managed by Orthopedics with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about panniculitis? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Periarthritis
periarthritis: An arthritis that is characterized by inflammation of the tissues surrounding a joint. It is a common cause of joint pain and stiffness.
Classification
Ontology identifier: DOID:2964 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › bone inflammation disease › arthritis.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: M77.9
- MeSH: D010489
- SNOMED CT: 50921008
Care at Weyland-Yutani Health System
Orthopedics specialists lead care for periarthritis. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Questions about periarthritis? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Polymyalgia rheumatica
polymyalgia rheumatica: A collagen disease that is characterized by pain, stiffness, and tenderness of the proximal muscle groups including the shoulder, pelvic girdle and the neck.
Classification
Ontology identifier: DOID:853 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › primary immunodeficiency disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: M35.3
- ICD-9-CM: 725
- MeSH: D011111
- SNOMED CT: 202834009
Care at Weyland-Yutani Health System
Orthopedics specialists lead care for polymyalgia rheumatica. 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 polymyalgia rheumatica. Bring a list of current medications and any previous test results.
Reference links
Psoriasis
psoriasis: A skin disease that is characterized by patches of thick red skin and silvery scales.
Classification
Ontology identifier: DOID:8893 (Human Disease Ontology).
Classification path: disease of anatomical entity › integumentary system disease › skin disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: L40
- MeSH: D011565
- OMIM: PS177900
- SNOMED CT: 156369008
Care at Weyland-Yutani Health System
Orthopedics specialists lead care for psoriasis. 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 psoriasis. Bring a list of current medications and any previous test results.
Reference links
Rickets
A bone remodeling disease that has_material_basis_in impaired mineralization or calcification of bones before epiphyseal closure due to deficiency or impaired metabolism of vitamin D, phosphorus or calcium which results_in softening and deformity located_in bone. Patients with rickets are cared for through our Orthopedics service line.
Also known as
Classification
Ontology identifier: DOID:10609 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › bone remodeling disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: E55.0
- MeSH: D012279
- SNOMED CT: 190639009
Care at Weyland-Yutani Health System
Orthopedics specialists lead care for rickets. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Questions about rickets? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Saethre-Chotzen syndrome
An acrocephalosyndactylia that has_material_basis_in a genetic mutation in the TWIST1 gene which results_in premature fusion located_in skull. This page summarizes how Saethre-Chotzen syndrome is classified and the care available at Weyland-Yutani Health System.
Classification
Ontology identifier: DOID:14768 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal dominant disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- MeSH: D000168
- OMIM: 101400
- OMIM: 180750
- SNOMED CT: 390726000
Care at Weyland-Yutani Health System
Treatment of Saethre-Chotzen 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
Questions about Saethre-Chotzen syndrome? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Short-rib thoracic dysplasia 10 with or without polydactyly
An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the IFT172 gene on chromosome 2p23. Our Orthopedics team evaluates and manages short-rib thoracic dysplasia 10 with or without polydactyly.
Also known as
Classification
Ontology identifier: DOID:0110091 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › bone development disease › asphyxiating thoracic dystrophy.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: Q77.2
- ICD-10-CM: Q87.5
- OMIM: 615630
Care at Weyland-Yutani Health System
Treatment of short-rib thoracic dysplasia 10 with or without polydactyly begins with an evaluation in Orthopedics. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
When to seek care
Questions about short-rib thoracic dysplasia 10 with or without polydactyly? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Short-rib thoracic dysplasia 11 with or without polydactyly
In clinical terms, short-rib thoracic dysplasia 11 with or without polydactyly is described as follows: an asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the WDR34 gene on chromosome 9q34.
Also known as
Classification
Ontology identifier: DOID:0110095 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › bone development disease › asphyxiating thoracic dystrophy.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: Q77.2
- OMIM: 615633
Care at Weyland-Yutani Health System
Treatment of short-rib thoracic dysplasia 11 with or without polydactyly 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
Seek a medical evaluation if you are concerned about short-rib thoracic dysplasia 11 with or without polydactyly. Bring a list of current medications and any previous test results.
Reference links
Short-rib thoracic dysplasia 13 with or without polydactyly
An asphyxiating thoracic dystrophy that has_material_basis_in homozygous mutation in the CEP120 gene on chromosome 5q23. This page summarizes how short-rib thoracic dysplasia 13 with or without polydactyly is classified and the care available at Weyland-Yutani Health System.
Also known as
Classification
Ontology identifier: DOID:0110093 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › bone development disease › asphyxiating thoracic dystrophy.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: Q77.2
- OMIM: 616300
Care at Weyland-Yutani Health System
Orthopedics specialists lead care for short-rib thoracic dysplasia 13 with or without polydactyly. 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 short-rib thoracic dysplasia 13 with or without polydactyly. Bring a list of current medications and any previous test results.
Reference links
Short-rib thoracic dysplasia 14 with polydactyly
Overview. An asphyxiating thoracic dystrophy that has_material_basis_in homozygous mutation in the KIAA0586 gene on chromosome 14q23. Weyland-Yutani Health System offers diagnosis and ongoing care for short-rib thoracic dysplasia 14 with polydactyly.
Also known as
Classification
Ontology identifier: DOID:0110096 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › bone development disease › asphyxiating thoracic dystrophy.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: Q04.3
- OMIM: 616546
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, short-rib thoracic dysplasia 14 with polydactyly is managed by Orthopedics with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
When to seek care
Questions about short-rib thoracic dysplasia 14 with polydactyly? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Short-rib thoracic dysplasia 6 with or without polydactyly
Overview. An asphyxiating thoracic dystrophy that has_material_basis_in homozygous mutation in the NEK1 gene on chromosome 4q33. Weyland-Yutani Health System offers diagnosis and ongoing care for short-rib thoracic dysplasia 6 with or without polydactyly.
Also known as
- Majewski syndrome
- polydactyly with neonatal chondrodystrophy, type II
- short rib-polydactyly syndrome type IIA
- SRPS2A
- SRTD6
Classification
Ontology identifier: DOID:0110092 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › bone development disease › asphyxiating thoracic dystrophy.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: Q77.2
- OMIM: 263520
Care at Weyland-Yutani Health System
Orthopedics specialists lead care for short-rib thoracic dysplasia 6 with or without polydactyly. 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 short-rib thoracic dysplasia 6 with or without polydactyly. Bring a list of current medications and any previous test results.
Reference links
Short-rib thoracic dysplasia 7 with or without polydactyly
Overview. An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the WDR35 gene on chromosome 2p21.1. Weyland-Yutani Health System offers diagnosis and ongoing care for short-rib thoracic dysplasia 7 with or without polydactyly.
Also known as
- short rib-polydactyly syndrome type V
- SRPS5
- SRTD7
Classification
Ontology identifier: DOID:0110090 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › bone development disease › asphyxiating thoracic dystrophy.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: Q77.2
- OMIM: 614091
Care at Weyland-Yutani Health System
Orthopedics specialists lead care for short-rib thoracic dysplasia 7 with or without polydactyly. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
Related articles
When to seek care
If you or a family member may have short-rib thoracic dysplasia 7 with or without polydactyly, contact your primary care provider or schedule a visit with Orthopedics.
Reference links
Short-rib thoracic dysplasia 8 with or without polydactyly
An asphyxiating thoracic dystrophy that has_material_basis_in compound heterozygous mutation in the WDR60 gene on chromosome 7q36. Patients with short-rib thoracic dysplasia 8 with or without polydactyly are cared for through our Orthopedics service line.
Also known as
- short rib-polydactyly syndrome type VI
- SRPS6
- SRTD8
Classification
Ontology identifier: DOID:0110094 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › bone development disease › asphyxiating thoracic dystrophy.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: Q77.2
- OMIM: 615503
Care at Weyland-Yutani Health System
Treatment of short-rib thoracic dysplasia 8 with or without polydactyly begins with an evaluation in Orthopedics. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
When to seek care
Questions about short-rib thoracic dysplasia 8 with or without polydactyly? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Smith-McCort dysplasia
In clinical terms, Smith-McCort dysplasia is described as follows: A Dyggve-Melchior-Clausen disease that is characterized by short limbs and a short trunk with a barrel-shaped chest.
Classification
Ontology identifier: DOID:0060247 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease › Dyggve-Melchior-Clausen disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- MeSH: C564589
- OMIM: PS607326
- SNOMED CT: 715862006
Care at Weyland-Yutani Health System
Care for Smith-McCort dysplasia 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 Smith-McCort dysplasia. Bring a list of current medications and any previous test results.
Reference links
Spondylolisthesis
Overview. A bone structure disease that has_material_basis_in displacement located_in set of vertebrae. Weyland-Yutani Health System offers diagnosis and ongoing care for spondylolisthesis.
Classification
Ontology identifier: DOID:6682 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › spinal disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: M43.1
- MeSH: D013168
- OMIM: 184200
- SNOMED CT: 157003009
Care at Weyland-Yutani Health System
Treatment of spondylolisthesis 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 spondylolisthesis, contact your primary care provider or schedule a visit with Orthopedics.
Reference links
Spondylolysis
A bone structure disease that involves a defect located_in lumbar vertebral column. Our Orthopedics team evaluates and manages spondylolysis.
Classification
Ontology identifier: DOID:2300 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › spinal disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: M43.0
- MeSH: D013169
- SNOMED CT: 203688008
Care at Weyland-Yutani Health System
Orthopedics specialists lead care for spondylolysis. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about spondylolysis? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Spondylometaphyseal dysplasia corner fracture type
A spondylometaphyseal dysplasia characterized by flake-like, triangular, or curvilinear ossification centers at the edges of irregular metaphyses that simulate fractures that has_material_basis_in heterozygous mutation in FN1 on chromosome 2q35. Patients with spondylometaphyseal dysplasia corner fracture type are cared for through our Orthopedics service line.
Also known as
- SMDCF
- spondylometaphyseal dysplasia Sutcliffe type
Classification
Ontology identifier: DOID:0112297 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal dominant disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- MeSH: C535793
- OMIM: 184255
- SNOMED CT: 254078005
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, spondylometaphyseal dysplasia corner fracture type is managed by Orthopedics with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
When to seek care
Questions about spondylometaphyseal dysplasia corner fracture type? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Syndactyly
In clinical terms, syndactyly is described as follows: A synostosis that results_in the fusion of two or more digits.
Also known as
- symphalangism
- symphalangy
- webbing of digits
Classification
Ontology identifier: DOID:11193 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › bone development disease › dysostosis › synostosis.
Specialty: Orthopedics
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: Q70
- ICD-9-CM: 755.1
- MeSH: D013576
- SNOMED CT: 156989004
Care at Weyland-Yutani Health System
Care for syndactyly 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 syndactyly. Bring a list of current medications and any previous test results.
Reference links
Syndactyly type 8
A syndactyly characterized by isolated fusion of the fourth and fifth metacarpals that has_material_basis_in hemizygous or homozygous mutation in the FGF16 gene on chromosome Xq21.1. Patients with syndactyly type 8 are cared for through our Orthopedics service line.
Also known as
- fusion of metacarpals 4 and 5
- metacarpal 4-5 fusion
Classification
Ontology identifier: DOID:0111813 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › X-linked monogenic disease › X-linked recessive disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- MeSH: C564100
- OMIM: 309630
- SNOMED CT: 715442006
Care at Weyland-Yutani Health System
Orthopedics specialists lead care for syndactyly type 8. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Questions about syndactyly type 8? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Synpolydactyly
A syndactyly characterized by an increased number of digits; often a result of a mutation in the HOXD13 gene. Patients with synpolydactyly are cared for through our Orthopedics service line.
Also known as
Classification
Ontology identifier: DOID:0060242 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › bone development disease › dysostosis › synostosis › syndactyly.
Specialty: Orthopedics
Broader conditions
Medical codes
- MeSH: C538153
- OMIM: 186000
- OMIM: 608180
- OMIM: 610234
- SNOMED CT: 715724002
Care at Weyland-Yutani Health System
Care for synpolydactyly 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 synpolydactyly. Bring a list of current medications and any previous test results.
Reference links