Orthopedics conditions, page 1 of 5
20 conditions on this page, alphabetically from Acrocephalosyndactylia to Charcot-Marie-Tooth disease type 4B2. Each entry below describes the condition in full.
On this page
Acrocephalosyndactylia
In clinical terms, acrocephalosyndactylia is described as follows: A synostosis that results_in craniosynostosis and syndactyly.
Also known as
Classification
Ontology identifier: DOID:12960 (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-9-CM: 755.55
- MeSH: D000168
- OMIM: 101200
- SNOMED CT: 205257004
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, acrocephalosyndactylia 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 acrocephalosyndactylia. Bring a list of current medications and any previous test results.
Reference links
Acrofacial dysostosis, Catania type
acrofacial dysostosis, Catania type: An acrofacial dysostosis that is characterized by intrauterine growth retardation, short stature, microcephaly, cleft palate, limb hypoplasia, simian creases and cryptorchidism/hypospadias.
Also known as
- Opitz Mollica Sorge syndrome
- Opitz-Caltabiano syndrome
Classification
Ontology identifier: DOID:0060384 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › bone development disease › dysostosis › acrofacial dysostosis.
Specialty: Orthopedics
Broader conditions
Medical codes
- MeSH: C538182
- OMIM: 101805
- SNOMED CT: 720419000
Care at Weyland-Yutani Health System
Treatment of acrofacial dysostosis, Catania type 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 acrofacial dysostosis, Catania type? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Acromicric dysplasia
Overview. An osteochondrodysplasia characterized by autosomal dominant inheritance of severe short stature, short hands and feet, joint limitations, mild facial anomalies, skin thickening, and bone abnormalities including delayed bone age, cone-shaped epiphyses, shortened long tubular bones, and ovoid vertebral bodies that has_material_basis_in heterozygous mutation in FBN1 on 15q21.1. Weyland-Yutani Health System offers diagnosis and ongoing care for acromicric dysplasia.
Also known as
- ACMICD
- acromicric skeletal dysplasia
Classification
Ontology identifier: DOID:0111243 (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
- MeSH: C535662
- OMIM: 102370
- SNOMED CT: 254090007
Care at Weyland-Yutani Health System
Orthopedics specialists lead care for acromicric dysplasia. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about acromicric dysplasia? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Alopecia areata
An autoimmune disease resulting in the loss of hair on the scalp and elsewhere on the body initially causing bald spots. Patients with alopecia areata are cared for through our Orthopedics service line.
Also known as
Classification
Ontology identifier: DOID:986 (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: L63
- ICD-9-CM: 704.01
- MeSH: D000506
- OMIM: 104000
- OMIM: 610753
- SNOMED CT: 201131001
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, alopecia areata is managed by Orthopedics with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
Related articles
When to seek care
If you or a family member may have alopecia areata, contact your primary care provider or schedule a visit with Orthopedics.
Reference links
Antley-Bixler syndrome with disordered steroidogenesis
An Antley-Bixler syndrome that is characterized at birth or prenatally by malformations and deformities affecting the majority of the skeleton and other areas of the body with autosomal recessive inheritance of the FGFR2 gene. Patients with Antley-Bixler syndrome with disordered steroidogenesis are cared for through our Orthopedics service line.
Also known as
- trapezoidocephaly-synostosis syndrome
Classification
Ontology identifier: DOID:0050462 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- OMIM: 201750
- SNOMED CT: 62964007
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, Antley-Bixler syndrome with disordered steroidogenesis is managed by Orthopedics with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
Related articles
When to seek care
Seek a medical evaluation if you are concerned about Antley-Bixler syndrome with disordered steroidogenesis. Bring a list of current medications and any previous test results.
Reference links
Arthropathy
In clinical terms, arthropathy is described as follows: A bone disease that is located_in the joint.
Also known as
- ankylosis of ankle and foot joint
- ankylosis of forearm joint
- ankylosis of hand joint
- Ankylosis of joint of ankle and/or foot
- Ankylosis of joint of forearm
- Ankylosis of joint of hand
- Ankylosis of joint of lower leg
- ankylosis of joint of multiple sites
- ankylosis of joint of pelvic region and thigh
- ankylosis of joint of shoulder region
- Ankylosis of joint of upper arm
- ankylosis of lower leg joint
- Ankylosis of multiple joints
- ankylosis of upper arm joint
- Infectious arthropathy
- Joint ankylosis of the ankle and foot
- Joint ankylosis of the ankle and/or foot
- Joint ankylosis of the forearm
- Joint ankylosis of the hand
- Joint ankylosis of the lower leg
- Joint ankylosis of the pelvic region and thigh
- Joint ankylosis of the shoulder region
- Joint ankylosis of the upper arm
Classification
Ontology identifier: DOID:381 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease.
Specialty: Orthopedics
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: M00-M02
- ICD-10-CM: M12.9
- ICD-9-CM: 711
- ICD-9-CM: 719.90
- MeSH: D007592
- SNOMED CT: 48548006
- SNOMED CT: 8316001
Care at Weyland-Yutani Health System
Treatment of arthropathy 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 arthropathy. Bring a list of current medications and any previous test results.
Reference links
Articular cartilage disease
A cartilage disease that is characterized by damage to the cartilage that covers the ends of the bones. Patients with articular cartilage disease are cared for through our Orthopedics service line.
Classification
Ontology identifier: DOID:6227 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › cartilage disease.
Specialty: Orthopedics
Broader conditions
More specific conditions
Medical codes
- ICD-9-CM: 718.0
- SNOMED CT: 268062001
Care at Weyland-Yutani Health System
Care for articular cartilage disease 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 articular cartilage disease? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Asphyxiating thoracic dystrophy
asphyxiating thoracic dystrophy: A bone development disease characterized by skeletal abnormalities and resulting in difficulty in breathing caused by mutations that result in ciliopathy.
Also known as
- Jeune syndrome
- short-rib thoracic dysplasia with or without polydactyly
- thoracic pelvic phalangeal dystrophy
Classification
Ontology identifier: DOID:0050592 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › bone development disease.
Specialty: Orthopedics
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: Q77.2
- OMIM: PS208500
Care at Weyland-Yutani Health System
Orthopedics specialists lead care for asphyxiating thoracic dystrophy. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about asphyxiating thoracic dystrophy? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Autosomal recessive type IV Ehlers-Danlos syndrome
In clinical terms, autosomal recessive type IV Ehlers-Danlos syndrome is described as follows: an Ehlers-Danlos syndrome that is characterized by the association of unexpected organ fragility (arterial/bowel/gravid uterine rupture) with inconstant physical features as thin, translucent skin, easy bruising and acrogeric traits.
Also known as
- Ehlers-Danlos syndrome, recessive type 4
Classification
Ontology identifier: DOID:14759 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease.
Specialty: Orthopedics
Broader conditions
Medical codes
Care at Weyland-Yutani Health System
Orthopedics specialists lead care for autosomal recessive type IV Ehlers-Danlos syndrome. 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 autosomal recessive type IV Ehlers-Danlos syndrome, contact your primary care provider or schedule a visit with Orthopedics.
Reference links
Bone disease
A connective tissue disease that affects the structure or development of bone or causes an impairment of normal bone function. Patients with bone disease are cared for through our Orthopedics service line.
Classification
Ontology identifier: DOID:0080001 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease.
Specialty: Orthopedics
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: M89.9
- MeSH: D001847
- SNOMED CT: 76069003
Care at Weyland-Yutani Health System
Care for bone disease 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 bone disease. Bring a list of current medications and any previous test results.
Reference links
Bone inflammation disease
bone inflammation disease: A bone disease that results_in inflammation of the located_in bone.
Also known as
- bone inflammatory disease
- Inflammatory disorder of bone
- osteitis
Classification
Ontology identifier: DOID:3342 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease.
Specialty: Orthopedics
Broader conditions
More specific conditions
Medical codes
- MeSH: D010000
- SNOMED CT: 274144001
Care at Weyland-Yutani Health System
Orthopedics specialists lead care for bone inflammation disease. 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 bone inflammation disease, contact your primary care provider or schedule a visit with Orthopedics.
Reference links
Caffey disease
A bone inflammation disease that causes bone changes, soft tissue swelling and irritability in infants. The disease has been associated with COL1A1 gene. It has symptom soft-tissue swelling, has symptom bone lesions, and has symptom irritability. Our Orthopedics team evaluates and manages Caffey disease.
Also known as
- cortical congenital hyperostosis
- infantile cortical hyperostosis
Classification
Ontology identifier: DOID:4257 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease › bone disease › bone inflammation disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: M89.8
- MeSH: D006958
- OMIM: 114000
- SNOMED CT: 24752008
Care at Weyland-Yutani Health System
Treatment of Caffey 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 Caffey disease? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Camurati-Engelmann disease
An osteosclerosis characterized by the cortical thickening of the diaphyses of the long bones. This page summarizes how Camurati-Engelmann disease is classified and the care available at Weyland-Yutani Health System.
Also known as
- Diaphyseal dysplasia
- Engelman's disease
- progressive diaphyseal dysplasia
Classification
Ontology identifier: DOID:4997 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: Q78.3
- MeSH: D003966
- OMIM: PS131300
- SNOMED CT: 34643004
Care at Weyland-Yutani Health System
Care for Camurati-Engelmann disease 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 Camurati-Engelmann disease. Bring a list of current medications and any previous test results.
Reference links
Cartilage disease
Overview. A connective tissue disease that is located_in cartilage. Weyland-Yutani Health System offers diagnosis and ongoing care for cartilage disease.
Also known as
- Cartilage disorder
- Chondropathy
Classification
Ontology identifier: DOID:1222 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › connective tissue disease.
Specialty: Orthopedics
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: M94.9
- MeSH: D002357
- SNOMED CT: 50927007
Care at Weyland-Yutani Health System
Care for cartilage disease 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 cartilage disease, contact your primary care provider or schedule a visit with Orthopedics.
Reference links
Charcot-Marie-Tooth disease
In clinical terms, Charcot-Marie-Tooth disease is described as follows: A neuromuscular disease that is characterized by a slowly progressive degeneration of the muscles of the foot, lower leg, hand and forearm.
Also known as
- CMT - Charcot-Marie-Tooth disease
- Hereditary sensory and motor neuropathy
Classification
Ontology identifier: DOID:10595 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › neuromuscular disease.
Specialty: Orthopedics
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: G60.0
- ICD-9-CM: 356.1
- MeSH: D002607
- OMIM: PS118220
- SNOMED CT: 193158000
Care at Weyland-Yutani Health System
Care for Charcot-Marie-Tooth disease 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 Charcot-Marie-Tooth disease. Bring a list of current medications and any previous test results.
Reference links
Charcot-Marie-Tooth disease axonal type 2L
Charcot-Marie-Tooth disease axonal type 2L: A Charcot-Marie-Tooth disease type 2 that has_material_basis_in mutation in the HSPB8 gene.
Also known as
- autosomal dominant axonal Charcot-Marie-Tooth disease type 2L
- autosomal dominant Charcot-Marie-Tooth disease type 2L
- Charcot-Marie-Tooth neuropathy axonal type 2L
- CMT2L
Classification
Ontology identifier: DOID:0110174 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › neuromuscular disease › Charcot-Marie-Tooth disease › Charcot-Marie-Tooth disease type 2.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: G60.0
- OMIM: 608673
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, Charcot-Marie-Tooth disease axonal type 2L is managed by Orthopedics with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
When to seek care
Questions about Charcot-Marie-Tooth disease axonal type 2L? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Charcot-Marie-Tooth disease recessive intermediate B
A Charcot-Marie-Tooth disease intermediate type that has_material_basis_in compound heterozygous mutation in the KARS gene on chromosome 16q23. Our Orthopedics team evaluates and manages Charcot-Marie-Tooth disease recessive intermediate B.
Also known as
- autosomal recessive intermediate Charcot-Marie-Tooth disease type B
- Charcot-Marie-Tooth neuropathy recessive intermediate B
- CMTRIB
- RI-CMTB
Classification
Ontology identifier: DOID:0110204 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › neuromuscular disease › Charcot-Marie-Tooth disease › Charcot-Marie-Tooth disease intermediate type.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: G60.0
- OMIM: 613641
Care at Weyland-Yutani Health System
Treatment of Charcot-Marie-Tooth disease recessive intermediate B 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 Charcot-Marie-Tooth disease recessive intermediate B? Call your nearest Weyland-Yutani location and ask for Orthopedics.
Reference links
Charcot-Marie-Tooth disease type 2A2A
A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the MFN2 gene on chromosome 1p36.22. Patients with Charcot-Marie-Tooth disease type 2A2A are cared for through our Orthopedics service line.
Also known as
- autosomal dominant axonal Charcot-Marie-Tooth disease type 2A2
- Charcot-Marie-Tooth neuronal type 2A2
- Charcot-Marie-Tooth neuropathy type 2A2
- CMT2A2A
- hereditary motor and sensory neuropathy IIA2
- HMSN IIA2
- HMSN2A2
Classification
Ontology identifier: DOID:0110155 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › neuromuscular disease › Charcot-Marie-Tooth disease › Charcot-Marie-Tooth disease type 2.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: G60.0
- OMIM: 609260
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, Charcot-Marie-Tooth disease type 2A2A is managed by Orthopedics with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
Related articles
When to seek care
Seek a medical evaluation if you are concerned about Charcot-Marie-Tooth disease type 2A2A. Bring a list of current medications and any previous test results.
Reference links
Charcot-Marie-Tooth disease type 2B1
Overview. A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous mutation in the lamin A/C gene (LMNA) on chromosome 1q22. Weyland-Yutani Health System offers diagnosis and ongoing care for Charcot-Marie-Tooth disease type 2B1.
Also known as
- autosomal recessive axonal Charcot-Marie-Tooth disease type 2B1
- autosomal recessive axonal CMT4C1
- autosomal recessive Charcot-Marie-Tooth disease type 2B1
- Charcot-Marie-Tooth disease neuronal type 2B1
- Charcot-Marie-Tooth neuropathy type 2B1
- CMT2B1
Classification
Ontology identifier: DOID:0110156 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › neuromuscular disease › Charcot-Marie-Tooth disease › Charcot-Marie-Tooth disease type 2.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: G60.0
- MeSH: C537990
- OMIM: 605588
Care at Weyland-Yutani Health System
Orthopedics specialists lead care for Charcot-Marie-Tooth disease type 2B1. 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 Charcot-Marie-Tooth disease type 2B1, contact your primary care provider or schedule a visit with Orthopedics.
Reference links
Charcot-Marie-Tooth disease type 4B2
A Charcot-Marie-Tooth disease type 4 that has_material_basis_in mutation in the SBF2 gene. Our Orthopedics team evaluates and manages Charcot-Marie-Tooth disease type 4B2.
Also known as
- autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B2
- Charcot-Marie-Tooth neuropathy type 4B2
- CMT4B2
Classification
Ontology identifier: DOID:0110190 (Human Disease Ontology).
Classification path: disease of anatomical entity › musculoskeletal system disease › neuromuscular disease › Charcot-Marie-Tooth disease › Charcot-Marie-Tooth disease type 4.
Specialty: Orthopedics
Broader conditions
Medical codes
- ICD-10-CM: G60.0
- MeSH: C535421
- OMIM: 604563
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, Charcot-Marie-Tooth disease type 4B2 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 Charcot-Marie-Tooth disease type 4B2. Bring a list of current medications and any previous test results.
Reference links