Neurology conditions, page 5 of 6
20 conditions on this page, alphabetically from Migraine with aura to Stiff-Person syndrome. Each entry below describes the condition in full.
On this page
Migraine with aura
A migraine characterized by migraine headache which is preceded or accompanied by a transient focal neurological phenomenon. Our Neurology team evaluates and manages migraine with aura.
Also known as
Classification
Ontology identifier: DOID:10024 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › brain disease › migraine.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G43.1
- ICD-9-CM: 346.0
- MeSH: D020325
- OMIM: 609179
- OMIM: 609670
- SNOMED CT: 155047002
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, migraine with aura is managed by Neurology with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
When to seek care
Questions about migraine with aura? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Motor peripheral neuropathy
A neuropathy that is characterized by inflammation or degeneration of the peripheral motor nerves. Our Neurology team evaluates and manages motor peripheral neuropathy.
Also known as
- neuropathic muscular atrophy
- Peripheral Motor Neuropathy
Classification
Ontology identifier: DOID:2477 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › peripheral nervous system disease › neuropathy.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G60.0
- MeSH: D015417
- SNOMED CT: 128202008
Care at Weyland-Yutani Health System
Neurology specialists lead care for motor peripheral 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 motor peripheral neuropathy, contact your primary care provider or schedule a visit with Neurology.
Reference links
Movement disease
movement disease: A brain disease that is characterized by a clinical syndrome of either hyperkinetic movement or hyperkinetic movement unrelated to weakness or spasticity.
Classification
Ontology identifier: DOID:480 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › brain disease.
Specialty: Neurology
Broader conditions
More specific conditions
Medical codes
- MeSH: D009069
- SNOMED CT: 60342002
Care at Weyland-Yutani Health System
Treatment of movement 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
Seek a medical evaluation if you are concerned about movement disease. Bring a list of current medications and any previous test results.
Reference links
Nervous system disease
A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system. Our Neurology team evaluates and manages nervous system disease.
Classification
Ontology identifier: DOID:863 (Human Disease Ontology).
Classification path: disease of anatomical entity.
Specialty: Neurology
More specific conditions
Medical codes
- ICD-10-CM: G98
- ICD-9-CM: 349.9
- MeSH: D009422
- SNOMED CT: 155262005
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, nervous system disease is managed by Neurology with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
When to seek care
Questions about nervous system disease? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Neurodegenerative disease
In clinical terms, neurodegenerative disease is described as follows: A central nervous system disease that results in the progressive deterioration of function or structure of neurons.
Also known as
Classification
Ontology identifier: DOID:1289 (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: G31.9
- MeSH: D019636
- SNOMED CT: 362975008
Care at Weyland-Yutani Health System
Treatment of neurodegenerative disease 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 neurodegenerative disease? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Neuropathy
A nervous system disease that is located_in nerves or nerve cells. Patients with neuropathy are cared for through our Neurology service line.
Also known as
Classification
Ontology identifier: DOID:870 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › peripheral nervous system disease.
Specialty: Neurology
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: G62.9
- SNOMED CT: 42658009
Care at Weyland-Yutani Health System
Care for neuropathy 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 neuropathy. Bring a list of current medications and any previous test results.
Reference links
Normal pressure hydrocephalus
Overview. A communicating hydrocephalus characterized by normal cerebrospinal fluid pressure, gait instability, cognitive decline, and impaired bladder control. Onset is usually in late adulthood. Weyland-Yutani Health System offers diagnosis and ongoing care for normal pressure hydrocephalus.
Also known as
- Low pressure hydrocephalus
- NPH
Classification
Ontology identifier: DOID:1572 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › brain disease › cerebral degeneration › hydrocephalus › communicating hydrocephalus.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G91.2
- ICD-9-CM: 331.5
- MeSH: D006850
- SNOMED CT: 30753002
Care at Weyland-Yutani Health System
Neurology specialists lead care for normal pressure hydrocephalus. 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 normal pressure hydrocephalus, contact your primary care provider or schedule a visit with Neurology.
Reference links
Nutritional optic neuropathy
An optic neuritis that is characterized by nutritional deficiency causing optic nerve dysfunction, has_symptom painless bilateral progressive decrease in visual acuity and color perception, and has_material_basis_in nuritional deficits, especially of folate and vitamin B, which can be associated with restrictive diets and alcohol abuse. Our Neurology team evaluates and manages nutritional optic neuropathy.
Classification
Ontology identifier: DOID:1209 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › peripheral nervous system disease › neuropathy › cranial nerve disease › optic nerve disease › optic neuritis.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H46.2
- ICD-9-CM: 377.33
- SNOMED CT: 82108004
Care at Weyland-Yutani Health System
Care for nutritional optic neuropathy 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
Seek a medical evaluation if you are concerned about nutritional optic neuropathy. Bring a list of current medications and any previous test results.
Reference links
Olivopontocerebellar atrophy
A neurodegenerative disease that is characterized by progressive cerebellar ataxia, leading to clumsiness in body movements, veering from midline when walking, wide-based stance, and falls without signs of paralysis or weakness and has_material_basis_in expansion of CAG triplet repeats (glutamine) resulting in degeneration of neuron in the cerebellum, pons and inferior olives. This page summarizes how olivopontocerebellar atrophy is classified and the care available at Weyland-Yutani Health System.
Also known as
- Dejerine-Thomas syndrome
- Thomas' syndrome
- WADIA-SWAMI SYNDROME
Classification
Ontology identifier: DOID:14784 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › neurodegenerative disease.
Specialty: Neurology
Broader conditions
Medical codes
- MeSH: D009849
- SNOMED CT: 67761004
Care at Weyland-Yutani Health System
Care for olivopontocerebellar atrophy 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
Seek a medical evaluation if you are concerned about olivopontocerebellar atrophy. Bring a list of current medications and any previous test results.
Reference links
Pontocerebellar hypoplasia
Overview. A neurodegenerative disease that is characterized by underdevelopment of the pons and cerebellum. Weyland-Yutani Health System offers diagnosis and ongoing care for pontocerebellar hypoplasia.
Also known as
Classification
Ontology identifier: DOID:0060264 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › neurodegenerative disease.
Specialty: Neurology
Broader conditions
More specific conditions
Medical codes
- MeSH: C580383
- OMIM: PS607596
- SNOMED CT: 45163000
Care at Weyland-Yutani Health System
Treatment of pontocerebellar hypoplasia 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 pontocerebellar hypoplasia, contact your primary care provider or schedule a visit with Neurology.
Reference links
Pontocerebellar hypoplasia type 6
A pontocerebellar hypoplasia that is characterized by olivopontocerebellar hypoplasia and developmental delay, has_material_basis_in autosomal recessive inheritance of mutation in the RARS2 gene. Our Neurology team evaluates and manages pontocerebellar hypoplasia type 6.
Classification
Ontology identifier: DOID:0060275 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › neurodegenerative disease › pontocerebellar hypoplasia.
Specialty: Neurology
Broader conditions
Medical codes
- MeSH: C548074
- OMIM: 611523
- SNOMED CT: 718606005
Care at Weyland-Yutani Health System
Treatment of pontocerebellar hypoplasia type 6 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
Seek a medical evaluation if you are concerned about pontocerebellar hypoplasia type 6. Bring a list of current medications and any previous test results.
Reference links
Pseudobulbar palsy
A brain disease that is characterized by damage to neurons of the corticobulbar tract, has_symptom dysarthria, has_symptom dysphagia, has_symptom spasticity located_in tongue, has_symptom gag reflex, and has_symptom emotional outbursts. Our Neurology team evaluates and manages pseudobulbar palsy.
Also known as
Classification
Ontology identifier: DOID:12680 (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-9-CM: 335.23
- MeSH: D020828
- SNOMED CT: 7379000
Care at Weyland-Yutani Health System
Care for pseudobulbar palsy 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 pseudobulbar palsy. Bring a list of current medications and any previous test results.
Reference links
Reflex epilepsy
A variable age at onset electroclinical syndrome that is consistently induced by identifiable and objective-specific triggers, which may be an afferent stimulus or by the patient's own activity. Our Neurology team evaluates and manages reflex epilepsy.
Also known as
- epilepsy, sensory-induced
Classification
Ontology identifier: DOID:2548 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › brain disease › epilepsy › electroclinical syndrome › variable age at onset electroclinical syndrome.
Specialty: Neurology
Broader conditions
Medical codes
- MeSH: D020195
- SNOMED CT: 79745005
Care at Weyland-Yutani Health System
Treatment of reflex epilepsy 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 reflex epilepsy. Bring a list of current medications and any previous test results.
Reference links
Restless legs syndrome
In clinical terms, restless legs syndrome is described as follows: A central nervous system disease characterized by throbbing, pulling creeping or other unpleasant sensations in the legs and the irresistible urge to move them.
Also known as
- WED
- Willis-Ekbom disease
- Wittmaack-Ekbom syndrome
Classification
Ontology identifier: DOID:0050425 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G25.81
- ICD-9-CM: 333.94
- MeSH: D012148
- OMIM: PS102300
- SNOMED CT: 32914008
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, restless legs syndrome 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 restless legs syndrome. Bring a list of current medications and any previous test results.
Reference links
Sensory peripheral neuropathy
A neuropathy that involves damage to sensory nerves of the peripheral nervous system. This page summarizes how sensory peripheral neuropathy is classified and the care available at Weyland-Yutani Health System.
Also known as
- peripheral Sensory Neuropathy
- sensory neuropathy
Classification
Ontology identifier: DOID:2491 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › peripheral nervous system disease › neuropathy.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-9-CM: 356.2
- MeSH: D009477
- SNOMED CT: 193163001
- SNOMED CT: 95662005
Care at Weyland-Yutani Health System
Care for sensory peripheral neuropathy 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 sensory peripheral neuropathy, contact your primary care provider or schedule a visit with Neurology.
Reference links
Sepiapterin reductase deficiency
sepiapterin reductase deficiency: A dystonia characterized by sustained muscle contractions with diurnal fluctuations, axial hypotonia, oculogyric crises, delays in motor and cognitive development and severe dopamine and serotonin deficiencies that has_material_basis_in mutation in the SPR gene on chromosome 2p resulting in sepiapterin reductase deficiency.
Also known as
- dopa-responsive dystonia due to sepiapterin reductase deficiency
- DRD due to SRD
- SPR deficiency
- SRD
Classification
Ontology identifier: DOID:0111168 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal dominant disease.
Specialty: Neurology
Broader conditions
Medical codes
- MeSH: C562657
- OMIM: 612716
- SNOMED CT: 1187545003
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, sepiapterin reductase deficiency 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 sepiapterin reductase deficiency, contact your primary care provider or schedule a visit with Neurology.
Reference links
Small fiber neuropathy
A neuropathy that solely or predominantly affects small myelinated A-delta (Aδ) fibers and unmyelinated C fibers resulting in sensory changes, autonomic dysfunction, or both. Common symptoms include burning, sharp and/or deep pain, allodynia, hyperalgesia, thermal and pinprick hypoesthesia, dry mouth, dry eyes, constipation, bladder incontinence, orthostatic dizziness, sexual dysfunction, red or white skin discoloration, or trouble sweating. Our Neurology team evaluates and manages small fiber neuropathy.
Also known as
Classification
Ontology identifier: DOID:0070701 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › peripheral nervous system disease › neuropathy.
Specialty: Neurology
Broader conditions
Medical codes
- MeSH: D000071075
- SNOMED CT: 709489006
Care at Weyland-Yutani Health System
Care for small fiber neuropathy 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
Questions about small fiber neuropathy? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Spastic diplegia
A spastic cerebral palsy that affects lower extremities resulting in tight leg and hip muscles. The legs cross at the knees, making it difficult to walk. Our Neurology team evaluates and manages spastic diplegia.
Also known as
- cerebral spastic infantile paralysis
- Diplegic infantile cerebral palsy
- infantile diplegic cerebral palsy
- Infantile spastic cerebral palsy
- Little's disease
- Littles disease
Classification
Ontology identifier: DOID:10965 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › brain disease › cerebral palsy › spastic cerebral palsy.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G80.1
- ICD-9-CM: 343.0
- MeSH: D002547
- SNOMED CT: 1178005
- SNOMED CT: 275469001
Care at Weyland-Yutani Health System
Neurology specialists lead care for spastic diplegia. 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 spastic diplegia. Bring a list of current medications and any previous test results.
Reference links
Spinal muscular atrophy with progressive myoclonic epilepsy
A motor neuron disease characterized by severe and progressive myoclonic epilepsy and lower-motor-neuron disease that has_material_basis_in homozygous or compound heterozygous mutation in the ASAH1 gene on chromosome 8p22. Our Neurology team evaluates and manages spinal muscular atrophy with progressive myoclonic epilepsy.
Also known as
- hereditary myoclonus-progressive distal muscular atrophy syndrome
- Jankovic-Rivera syndrome
- SMA-PME
- SMAPME
Classification
Ontology identifier: DOID:0111527 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease.
Specialty: Neurology
Broader conditions
Medical codes
- MeSH: C537563
- OMIM: 159950
- SNOMED CT: 703524005
Care at Weyland-Yutani Health System
Care for spinal muscular atrophy with progressive myoclonic epilepsy 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
Questions about spinal muscular atrophy with progressive myoclonic epilepsy? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Stiff-Person syndrome
A movement disease that is of unknown etiology characterized by progressive rigidity. Patients with Stiff-Person syndrome are cared for through our Neurology service line.
Also known as
- stiff man syndrome
- Stiff-man syndrome
Classification
Ontology identifier: DOID:13366 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › brain disease › movement disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G25.82
- ICD-9-CM: 333.91
- MeSH: D016750
- OMIM: 184850
- SNOMED CT: 5217008
Care at Weyland-Yutani Health System
Neurology specialists lead care for Stiff-Person syndrome. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Questions about Stiff-Person syndrome? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links