Neurology conditions, page 2 of 6
20 conditions on this page, alphabetically from Autosomal recessive nonsyndromic deafness 13 to Central pontine myelinolysis. Each entry below describes the condition in full.
On this page
Autosomal recessive nonsyndromic deafness 13
An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 7q34-q36. Our Neurology team evaluates and manages autosomal recessive nonsyndromic deafness 13.
Also known as
- autosomal recessive deafness 13
- DFNB13
Classification
Ontology identifier: DOID:0110468 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease › nonsyndromic deafness › autosomal recessive nonsyndromic deafness.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H90.3
- OMIM: 603098
Care at Weyland-Yutani Health System
Neurology specialists lead care for autosomal recessive nonsyndromic deafness 13. 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 autosomal recessive nonsyndromic deafness 13, contact your primary care provider or schedule a visit with Neurology.
Reference links
Autosomal recessive nonsyndromic deafness 17
An autosomal recessive nonsyndromic deafness that has_material_basis_in variation between D7S2453 and D7S525 in the chromosome region 7q31. This page summarizes how autosomal recessive nonsyndromic deafness 17 is classified and the care available at Weyland-Yutani Health System.
Also known as
- autosomal recessive deafness 17
- DFNB17
Classification
Ontology identifier: DOID:0110472 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease › nonsyndromic deafness › autosomal recessive nonsyndromic deafness.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H90.3
- OMIM: 603010
Care at Weyland-Yutani Health System
Treatment of autosomal recessive nonsyndromic deafness 17 begins with an evaluation in Neurology. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
When to seek care
If you or a family member may have autosomal recessive nonsyndromic deafness 17, contact your primary care provider or schedule a visit with Neurology.
Reference links
Autosomal recessive nonsyndromic deafness 29
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the CLDN14 gene on chromosome 21q22. Our Neurology team evaluates and manages autosomal recessive nonsyndromic deafness 29.
Also known as
- autosomal recessive deafness 29
- DFNB29
Classification
Ontology identifier: DOID:0110487 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease › nonsyndromic deafness › autosomal recessive nonsyndromic deafness.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H90.3
- OMIM: 614035
Care at Weyland-Yutani Health System
Neurology specialists lead care for autosomal recessive nonsyndromic deafness 29. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
Related articles
When to seek care
Seek a medical evaluation if you are concerned about autosomal recessive nonsyndromic deafness 29. Bring a list of current medications and any previous test results.
Reference links
Autosomal recessive nonsyndromic deafness 33
Overview. An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 10p11.23-q21.1. Weyland-Yutani Health System offers diagnosis and ongoing care for autosomal recessive nonsyndromic deafness 33.
Also known as
- autosomal recessive deafness 33
- DFNB33
Classification
Ontology identifier: DOID:0110492 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease › nonsyndromic deafness › autosomal recessive nonsyndromic deafness.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H90.3
- OMIM: 607239
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, autosomal recessive nonsyndromic deafness 33 is managed by Neurology 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 autosomal recessive nonsyndromic deafness 33. Bring a list of current medications and any previous test results.
Reference links
Autosomal recessive nonsyndromic deafness 4
autosomal recessive nonsyndromic deafness 4: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the SLC26A4 gene on chromosome 7q22.
Also known as
- autosomal recessive deafness 4 with enlarged vestibular aqueduct
- DFNB4
Classification
Ontology identifier: DOID:0110498 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease › nonsyndromic deafness › autosomal recessive nonsyndromic deafness.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H90.3
- OMIM: 600791
Care at Weyland-Yutani Health System
Treatment of autosomal recessive nonsyndromic deafness 4 begins with an evaluation in Neurology. 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 autosomal recessive nonsyndromic deafness 4. Bring a list of current medications and any previous test results.
Reference links
Autosomal recessive nonsyndromic deafness 44
autosomal recessive nonsyndromic deafness 44: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the ADCY1 gene on chromosome 7p12.
Also known as
- autosomal recessive deafness 44
- DFNB44
Classification
Ontology identifier: DOID:0110501 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease › nonsyndromic deafness › autosomal recessive nonsyndromic deafness.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H90.3
- OMIM: 610154
Care at Weyland-Yutani Health System
Treatment of autosomal recessive nonsyndromic deafness 44 begins with an evaluation in Neurology. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about autosomal recessive nonsyndromic deafness 44? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Autosomal recessive nonsyndromic deafness 47
An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 2p25.1-p24.3. Patients with autosomal recessive nonsyndromic deafness 47 are cared for through our Neurology service line.
Also known as
- autosomal recessive deafness 47
- DFNB47
Classification
Ontology identifier: DOID:0110504 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease › nonsyndromic deafness › autosomal recessive nonsyndromic deafness.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H90.3
- OMIM: 609946
Care at Weyland-Yutani Health System
Treatment of autosomal recessive nonsyndromic deafness 47 begins with an evaluation in Neurology. 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 autosomal recessive nonsyndromic deafness 47, contact your primary care provider or schedule a visit with Neurology.
Reference links
Autosomal recessive nonsyndromic deafness 83
In clinical terms, autosomal recessive nonsyndromic deafness 83 is described as follows: an autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 9p23-p21.2.
Also known as
- autosomal recessive deafness 83
- DFNB83
Classification
Ontology identifier: DOID:0110528 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease › nonsyndromic deafness › autosomal recessive nonsyndromic deafness.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H90.3
- OMIM: 613685
Care at Weyland-Yutani Health System
Care for autosomal recessive nonsyndromic deafness 83 is coordinated through Neurology. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
When to seek care
If you or a family member may have autosomal recessive nonsyndromic deafness 83, contact your primary care provider or schedule a visit with Neurology.
Reference links
Autosomal recessive nonsyndromic deafness 98
Overview. An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TSPEAR gene on chromosome 21q22. Weyland-Yutani Health System offers diagnosis and ongoing care for autosomal recessive nonsyndromic deafness 98.
Also known as
- autosomal recessive deafness 98
- DFNB98
Classification
Ontology identifier: DOID:0110540 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease › nonsyndromic deafness › autosomal recessive nonsyndromic deafness.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H90.3
- OMIM: 614861
Care at Weyland-Yutani Health System
Neurology specialists lead care for autosomal recessive nonsyndromic deafness 98. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
Related articles
When to seek care
Seek a medical evaluation if you are concerned about autosomal recessive nonsyndromic deafness 98. Bring a list of current medications and any previous test results.
Reference links
Basal ganglia calcification
Overview. A basal ganglia disease characterized by the presence of abnormal calcium deposits of unknown cause in the brain; has symptom dementia, psychosis, mood swings and loss of acquired motor skills. Weyland-Yutani Health System offers diagnosis and ongoing care for basal ganglia calcification.
Also known as
Classification
Ontology identifier: DOID:0060230 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › brain disease › basal ganglia disease.
Specialty: Neurology
Broader conditions
Medical codes
- MeSH: C536275
- OMIM: 114100
- OMIM: 213600
- OMIM: 615007
- OMIM: 615483
- SNOMED CT: 110997000
Care at Weyland-Yutani Health System
Treatment of basal ganglia calcification begins with an evaluation in Neurology. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about basal ganglia calcification? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Bell's palsy
In clinical terms, Bell's palsy is described as follows: A facial paralysis resulting from dysfunction in the cranial nerve VII (facial nerve).
Also known as
- Bell palsy
- Bell's (facial) palsy
Classification
Ontology identifier: DOID:12506 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › peripheral nervous system disease › neuropathy › cranial nerve disease › facial nerve disease › facial paralysis.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G51.0
- ICD-9-CM: 351.0
- MeSH: D020330
- SNOMED CT: 193093009
Care at Weyland-Yutani Health System
Treatment of Bell's palsy begins with an evaluation in Neurology. 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 Bell's palsy, contact your primary care provider or schedule a visit with Neurology.
Reference links
Bilateral optic nerve hypoplasia
An optic nerve disease characterized by isolated optic nerve hypoplasia or aplasia that has_material_basis_in heterozygous mutation in the PAX6 gene on chromosome 11p13. Our Neurology team evaluates and manages bilateral optic nerve hypoplasia.
Also known as
- familial bilateral optic nerve hypoplasia
- isolated optic nerve hypoplasia/aplasia
- ONH
Classification
Ontology identifier: DOID:0111531 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal dominant disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H47.03
- ICD-9-CM: 377.43
- MeSH: D000080344
- OMIM: 165550
- SNOMED CT: 95499004
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, bilateral optic nerve hypoplasia is managed by Neurology with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
When to seek care
If you or a family member may have bilateral optic nerve hypoplasia, contact your primary care provider or schedule a visit with Neurology.
Reference links
Brachial plexus neuritis
brachial plexus neuritis: A brachial plexus neuropathy that affects the chest, shoulder, arm and hand.
Also known as
- Brachial neuritis
- Parsonage-Aldren-Turner syndrome
Classification
Ontology identifier: DOID:3689 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › peripheral nervous system disease › neuropathy › neuritis.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G54.5
- MeSH: D020968
- SNOMED CT: 26609002
Care at Weyland-Yutani Health System
Care for brachial plexus neuritis is coordinated through Neurology. 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 brachial plexus neuritis? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Brachial plexus neuropathy
A peripheral nervous system disease that is characterized by damage to nerves in the upper shoulder of the brachial plexus, an area where nerves from the spinal cord branch into the arm nerves. Our Neurology team evaluates and manages brachial plexus neuropathy.
Also known as
- brachial plexopathy
- Brachial plexus disorder
Classification
Ontology identifier: DOID:3690 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › peripheral nervous system disease › neuropathy.
Specialty: Neurology
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: G54.0
- MeSH: D020516
- SNOMED CT: 3548001
Care at Weyland-Yutani Health System
Neurology specialists lead care for brachial plexus neuropathy. 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 brachial plexus neuropathy, contact your primary care provider or schedule a visit with Neurology.
Reference links
Brain disease
brain disease: A central nervous system disease that is located_in the brain.
Also known as
Classification
Ontology identifier: DOID:936 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease.
Specialty: Neurology
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: G93.40
- ICD-10-CM: G93.9
- ICD-9-CM: 348.30
- ICD-9-CM: 348.9
- MeSH: D001927
- SNOMED CT: 81308009
Care at Weyland-Yutani Health System
Care for brain disease is coordinated through Neurology. 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 brain disease. Bring a list of current medications and any previous test results.
Reference links
Brain edema
In clinical terms, brain edema is described as follows: A brain disease that is characterized by excess accumulation of fluid in the intracellular and/or extracellular spaces of the brain, has_symptom nausea, has_symptom vomiting, has_symptom blurred vision, has_symptom seizure, has_symptom coma.
Also known as
- intracranial swelling
- wet brain
Classification
Ontology identifier: DOID:4724 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › brain disease.
Specialty: Neurology
Broader conditions
Medical codes
- MeSH: D001929
- SNOMED CT: 85974009
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, brain edema is managed by Neurology with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
When to seek care
If you or a family member may have brain edema, contact your primary care provider or schedule a visit with Neurology.
Reference links
Cauda equina syndrome
A peripheral nervous system disease that involves an acute loss of function of the lumbar plexus, neurologic elements (nerve roots) of the spinal canal below the termination (conus) of the spinal cord. This page summarizes how Cauda equina syndrome is classified and the care available at Weyland-Yutani Health System.
Classification
Ontology identifier: DOID:11577 (Human Disease Ontology).
Classification path: syndrome.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G83.4
- ICD-9-CM: 344.6
- MeSH: D000077684
- SNOMED CT: 89356000
Care at Weyland-Yutani Health System
Treatment of Cauda equina syndrome begins with an evaluation in Neurology. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about Cauda equina syndrome? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Central nervous system disease
A nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system. Our Neurology team evaluates and manages central nervous system disease.
Classification
Ontology identifier: DOID:331 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease.
Specialty: Neurology
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: G96.9
- MeSH: D002493
- SNOMED CT: 267144009
Care at Weyland-Yutani Health System
Treatment of central nervous system disease begins with an evaluation in Neurology. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about central nervous system disease? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Central nervous system origin vertigo
A brain disease that is characterized by vertigo caused by hemorrhagic insult, ischemic insult or mass lesion of the cerebellum, the vestibular nuclei, and the brainstem, has_symptom dizziness, has_symptom nausea, has_symptom vomiting and has_symptom difficulty walking. This page summarizes how central nervous system origin vertigo is classified and the care available at Weyland-Yutani Health System.
Also known as
- central vestibular vertigo
- Vertigo of central origin
Classification
Ontology identifier: DOID:2479 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › brain disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H81.4
- ICD-9-CM: 386.2
- MeSH: D014717
- SNOMED CT: 20425006
Care at Weyland-Yutani Health System
Treatment of central nervous system origin vertigo begins with an evaluation in Neurology. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
When to seek care
Questions about central nervous system origin vertigo? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Central pontine myelinolysis
A demyelination disease that is characterized by severe damage to the myelin sheath of the pons' nerve cells and has_symptom acute paralysis, has_symptom dysphagia, and has_symptom dysarthria. Our Neurology team evaluates and manages central pontine myelinolysis.
Also known as
- osmotic demyelination syndrome
Classification
Ontology identifier: DOID:636 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › demyelinating disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G37.2
- MeSH: D017590
- SNOMED CT: 6807001
Care at Weyland-Yutani Health System
Care for central pontine myelinolysis is coordinated through Neurology. 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 central pontine myelinolysis. Bring a list of current medications and any previous test results.
Reference links