Ophthalmology conditions, page 4 of 4
13 conditions on this page, alphabetically from Retinitis pigmentosa 55 to Xerophthalmia. Each entry below describes the condition in full.
On this page
Retinitis pigmentosa 55
Overview. A retinitis pigmentosa that has_material_basis_in mutation in the ARL6 gene on chromosome 3q11.2. Weyland-Yutani Health System offers diagnosis and ongoing care for retinitis pigmentosa 55.
Also known as
Classification
Ontology identifier: DOID:0110370 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › eye disease › retinal disease › retinal degeneration › retinitis pigmentosa.
Specialty: Ophthalmology
Broader conditions
Medical codes
- ICD-10-CM: H35.5
- OMIM: 613575
Care at Weyland-Yutani Health System
Treatment of retinitis pigmentosa 55 begins with an evaluation in Ophthalmology. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about retinitis pigmentosa 55. Bring a list of current medications and any previous test results.
Reference links
Retinitis pigmentosa 57
retinitis pigmentosa 57: A retinitis pigmentosa that has_material_basis_in mutation in the PDE6G gene on chromosome 17q25.3.
Also known as
Classification
Ontology identifier: DOID:0110407 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease.
Specialty: Ophthalmology
Broader conditions
Medical codes
- ICD-10-CM: H35.5
- OMIM: 613582
Care at Weyland-Yutani Health System
Ophthalmology specialists lead care for retinitis pigmentosa 57. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
If you or a family member may have retinitis pigmentosa 57, contact your primary care provider or schedule a visit with Ophthalmology.
Reference links
Retinitis pigmentosa 66
In clinical terms, retinitis pigmentosa 66 is described as follows: A retinitis pigmentosa that has_material_basis_in mutation in the RBP3 gene on chromosome 10q11.
Also known as
Classification
Ontology identifier: DOID:0110393 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › eye disease › retinal disease › retinal degeneration › retinitis pigmentosa.
Specialty: Ophthalmology
Broader conditions
Medical codes
- ICD-10-CM: H35.5
- OMIM: 615233
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, retinitis pigmentosa 66 is managed by Ophthalmology with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
When to seek care
Questions about retinitis pigmentosa 66? Call your nearest Weyland-Yutani location and ask for Ophthalmology.
Reference links
Retinitis pigmentosa 9
retinitis pigmentosa 9: A retinitis pigmentosa that has_material_basis_in mutation in the RP9 gene on chromosome 7p14.
Also known as
Classification
Ontology identifier: DOID:0110387 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal dominant disease.
Specialty: Ophthalmology
Broader conditions
Medical codes
- ICD-10-CM: H35.5
- MeSH: C566716
- OMIM: 180104
Care at Weyland-Yutani Health System
Treatment of retinitis pigmentosa 9 begins with an evaluation in Ophthalmology. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
When to seek care
Questions about retinitis pigmentosa 9? Call your nearest Weyland-Yutani location and ask for Ophthalmology.
Reference links
Retinitis pigmentosa Y-linked
In clinical terms, retinitis pigmentosa Y-linked is described as follows: A retinitis pigmentosa that has_material_basis_in variation on the Y chromosome.
Classification
Ontology identifier: DOID:0110418 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › Y-linked monogenic disease.
Specialty: Ophthalmology
Broader conditions
Medical codes
- ICD-10-CM: H35.5
- OMIM: 400004
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, retinitis pigmentosa Y-linked is managed by Ophthalmology 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 retinitis pigmentosa Y-linked, contact your primary care provider or schedule a visit with Ophthalmology.
Reference links
Scleral disease
An eye disease that affects the sclera, which is the white fibrous outer layer of the eyeball. This page summarizes how scleral disease is classified and the care available at Weyland-Yutani Health System.
Classification
Ontology identifier: DOID:11343 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › eye disease.
Specialty: Ophthalmology
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: H15
- MeSH: D015422
- SNOMED CT: 33064008
Care at Weyland-Yutani Health System
Ophthalmology specialists lead care for scleral disease. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about scleral disease? Call your nearest Weyland-Yutani location and ask for Ophthalmology.
Reference links
Siderosis of eye
siderosis of eye: An eye degenerative disease that is characterized by intraocular iron toxicity typically due to a retained foreign body.
Also known as
Classification
Ontology identifier: DOID:11754 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › eye disease › eye degenerative disease.
Specialty: Ophthalmology
Broader conditions
Medical codes
- ICD-10-CM: H44.32
- ICD-9-CM: 360.23
- SNOMED CT: 25277000
Care at Weyland-Yutani Health System
Care for siderosis of eye is coordinated through Ophthalmology. 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 siderosis of eye. Bring a list of current medications and any previous test results.
Reference links
Strabismic amblyopia
In clinical terms, strabismic amblyopia is described as follows: an amblyopia that is characterized by strabismus or eye misalignment. The brain begins to ignore the eye that is not straight and the vision subsequently drops in that eye.
Also known as
Classification
Ontology identifier: DOID:10375 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › eye disease › amblyopia.
Specialty: Ophthalmology
Broader conditions
Medical codes
- ICD-10-CM: H53.03
- ICD-9-CM: 368.01
- MeSH: D000550
- SNOMED CT: 35600002
Care at Weyland-Yutani Health System
Ophthalmology specialists lead care for strabismic amblyopia. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Questions about strabismic amblyopia? Call your nearest Weyland-Yutani location and ask for Ophthalmology.
Reference links
Strabismus
In clinical terms, strabismus is described as follows: A hyperopia that is characterized by eyes that do not properly align with each other when looking at an object.
Classification
Ontology identifier: DOID:540 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › eye disease › ocular motility disease.
Specialty: Ophthalmology
Broader conditions
Medical codes
- ICD-10-CM: H50.8
- ICD-9-CM: 378.7
- SNOMED CT: 194125000
Care at Weyland-Yutani Health System
Care for strabismus is coordinated through Ophthalmology. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about strabismus? Call your nearest Weyland-Yutani location and ask for Ophthalmology.
Reference links
Subepithelial mucinous corneal dystrophy
subepithelial mucinous corneal dystrophy: An epithelial and subepithelial dystrophy that is characterized by frequent, recurrent corneal erosions in the first decade of life.
Also known as
Classification
Ontology identifier: DOID:0060454 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › eye disease › corneal disease › corneal dystrophy › epithelial and subepithelial dystrophy.
Specialty: Ophthalmology
Broader conditions
Medical codes
- ICD-10-CM: H18.5
- MeSH: C567547
- OMIM: 612867
Care at Weyland-Yutani Health System
Treatment of subepithelial mucinous corneal dystrophy begins with an evaluation in Ophthalmology. 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 subepithelial mucinous corneal dystrophy. Bring a list of current medications and any previous test results.
Reference links
Uveal disease
In clinical terms, uveal disease is described as follows: an eye disease affecting the uvea, which are the pigmented layers of the eye consisting of the iris, ciliary body, and choroid.
Classification
Ontology identifier: DOID:3480 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › eye disease.
Specialty: Ophthalmology
Broader conditions
More specific conditions
Medical codes
- MeSH: D014603
- SNOMED CT: 95678007
Care at Weyland-Yutani Health System
Care for uveal disease is coordinated through Ophthalmology. 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 uveal disease, contact your primary care provider or schedule a visit with Ophthalmology.
Reference links
Vitreous disease
vitreous disease: An eye and adnexa disease that is located in the vitreous of the eye.
Classification
Ontology identifier: DOID:9720 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › eye disease.
Specialty: Ophthalmology
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: H43.39
- ICD-9-CM: 379.24
- SNOMED CT: 194154006
Care at Weyland-Yutani Health System
Care for vitreous disease is coordinated through Ophthalmology. 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 vitreous disease. Bring a list of current medications and any previous test results.
Reference links
Xerophthalmia
Overview. A dry eye syndrome that is characterized by conjunctival and corneal xerosis, Bitot's spots, keratomalacia, nyctalopia, and retinopathy resulting from vitamin A deficiency. Weyland-Yutani Health System offers diagnosis and ongoing care for xerophthalmia.
Also known as
Classification
Ontology identifier: DOID:10138 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › eye disease › lacrimal apparatus disease › dry eye syndrome.
Specialty: Ophthalmology
Broader conditions
Medical codes
- ICD-10-CM: E50.7
- ICD-9-CM: 375.15
- MeSH: D014985
- SNOMED CT: 193887002
Care at Weyland-Yutani Health System
Ophthalmology specialists lead care for xerophthalmia. 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 xerophthalmia. Bring a list of current medications and any previous test results.
Reference links