Neurology conditions, page 1 of 6
20 conditions on this page, alphabetically from Acute hemorrhagic leukoencephalitis to Autosomal dominant nonsyndromic deafness 53. Each entry below describes the condition in full.
On this page
Acute hemorrhagic leukoencephalitis
A very rare form of acute disseminated encephalomyelitis, characterized by a brief but intense attack of inflammation and necrotizing vasculitis of venules and hemorrhage, and edema. This page summarizes how acute hemorrhagic leukoencephalitis is classified and the care available at Weyland-Yutani Health System.
Also known as
- acute haemorrhagic leucoencephalitis of Weston Hurst
- acute hemorrhagic encephalomyelitis
- acute necrotizing hemorrhagic leukoencephalitis
- AHL
- Weston-Hurst syndrome
Classification
Ontology identifier: DOID:10992 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › encephalomyelitis › acute disseminated encephalomyelitis.
Specialty: Neurology
Broader conditions
Medical codes
- MeSH: D004684
- OMIM: 606752
- SNOMED CT: 72986009
Care at Weyland-Yutani Health System
Care for acute hemorrhagic leukoencephalitis 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 acute hemorrhagic leukoencephalitis, contact your primary care provider or schedule a visit with Neurology.
Reference links
Adhesive otitis media
An auditory system disease that is characterized by a thin retracted ear drum becomes sucked into the middle-ear space and stuck (i.e., adherent) to the ossicles and other bones of the middle ear. This page summarizes how adhesive otitis media is classified and the care available at Weyland-Yutani Health System.
Also known as
- chronic adhesive otitis media
Classification
Ontology identifier: DOID:11235 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H74.1
- ICD-9-CM: 385.1
- SNOMED CT: 7699004
Care at Weyland-Yutani Health System
Treatment of adhesive otitis media 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 adhesive otitis media. Bring a list of current medications and any previous test results.
Reference links
Akinetic mutism
A brain disease characterized by marked reduction of nearly all motor functions including facial expressions, gestures and speech output, but with some degree of alertness. Patients with akinetic mutism are cared for through our Neurology service line.
Also known as
Classification
Ontology identifier: DOID:4267 (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: D000405
- SNOMED CT: 53333005
Care at Weyland-Yutani Health System
Care for akinetic mutism 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 akinetic mutism. Bring a list of current medications and any previous test results.
Reference links
Alexander disease
Overview. A leukodystrophy that is characterized by the destruction of white matter and the formation of Rosenthal fibers consisting of abnormal clumps of protein that accumulate in astrocytes. Weyland-Yutani Health System offers diagnosis and ongoing care for Alexander disease.
Also known as
Classification
Ontology identifier: DOID:4252 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal dominant disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G31.86
- MeSH: D038261
- OMIM: 203450
- SNOMED CT: 81854007
Care at Weyland-Yutani Health System
Treatment of Alexander 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
Seek a medical evaluation if you are concerned about Alexander disease. Bring a list of current medications and any previous test results.
Reference links
Alzheimer's disease
In clinical terms, Alzheimer's disease is described as follows: A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.
Also known as
- Alzheimer disease
- Alzheimers dementia
Classification
Ontology identifier: DOID:10652 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › neurodegenerative disease › tauopathy.
Specialty: Neurology
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: G30
- ICD-9-CM: 331.0
- MeSH: D000544
- SNOMED CT: 73768007
Care at Weyland-Yutani Health System
Neurology specialists lead care for Alzheimer's disease. 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 Alzheimer's disease, contact your primary care provider or schedule a visit with Neurology.
Reference links
Alzheimer's disease 10
Overview. An Alzheimer's disease that is characterized by an associated with variation in the region 7q36. Weyland-Yutani Health System offers diagnosis and ongoing care for Alzheimer's disease 10.
Also known as
- AD10
- Alzheimer disease 10
- Alzheimer disease familial 10
- Alzheimer's disease 10, early onset
Classification
Ontology identifier: DOID:0110043 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › neurodegenerative disease › tauopathy › Alzheimer's disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G30
- OMIM: 609636
Care at Weyland-Yutani Health System
Neurology specialists lead care for Alzheimer's disease 10. 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 Alzheimer's disease 10, contact your primary care provider or schedule a visit with Neurology.
Reference links
Alzheimer's disease 13
An Alzheimer's disease that is characterized by an associated with variation in the region 1q21. This page summarizes how Alzheimer's disease 13 is classified and the care available at Weyland-Yutani Health System.
Also known as
- AD13
- Alzheimer disease 13
- Alzheimer's disease 13, late onset
Classification
Ontology identifier: DOID:0110046 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › neurodegenerative disease › tauopathy › Alzheimer's disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G30
- OMIM: 611152
Care at Weyland-Yutani Health System
Neurology specialists lead care for Alzheimer's disease 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 Alzheimer's disease 13, contact your primary care provider or schedule a visit with Neurology.
Reference links
Alzheimer's disease 5
An Alzheimer's disease that is characterized by an associated with variation in the region 12p11.23-q13.12. This page summarizes how Alzheimer's disease 5 is classified and the care available at Weyland-Yutani Health System.
Also known as
- AD5
- Alzheimer disease 5
- Alzheimer disease, familial 5
- Alzheimer's disease 5, late onset
Classification
Ontology identifier: DOID:0110037 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal dominant disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G30
- OMIM: 602096
Care at Weyland-Yutani Health System
Treatment of Alzheimer's disease 5 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 Alzheimer's disease 5? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Amyotrophic lateral sclerosis type 4
An amyotrophic lateral sclerosis with juvenile onset that has_material_basis_in mutation in the SETX gene on chromosome 9. Patients with amyotrophic lateral sclerosis type 4 are cared for through our Neurology service line.
Also known as
- ALS4
- amyotrophic lateral sclerosis 4
- amyotrophic lateral sclerosis 4, juvenile
- dHMN with upper motor neuron signs
- distal hereditary motor neuropathy with pyramidal features
- distal hereditary motor neuropathy with upper motor neuron signs
Classification
Ontology identifier: DOID:0060196 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › neurodegenerative disease › motor neuron disease › amyotrophic lateral sclerosis.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G12.2
- OMIM: 602433
Care at Weyland-Yutani Health System
Neurology specialists lead care for amyotrophic lateral sclerosis type 4. 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 amyotrophic lateral sclerosis type 4, contact your primary care provider or schedule a visit with Neurology.
Reference links
Amyotrophic neuralgia
A brachial plexus neuropathy that is characterized by acute, recurrent episodes of brachial plexus neuropathy with muscle weakness and atrophy preceded by severe pain in the affected arm, and that has_material_basis_in heterozygous mutation in the SEPT9 gene on chromosome 17q25. This page summarizes how amyotrophic neuralgia is classified and the care available at Weyland-Yutani Health System.
Also known as
Classification
Ontology identifier: DOID:10383 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal dominant disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G54.5
- ICD-9-CM: 353.5
- MeSH: D020968
- OMIM: 162100
- SNOMED CT: 3548001
Care at Weyland-Yutani Health System
Treatment of amyotrophic neuralgia 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 amyotrophic neuralgia, contact your primary care provider or schedule a visit with Neurology.
Reference links
Anencephaly
A congenital nervous system abnormality characterized by failure of the anterior neuropore to close resulting in partial or complete absence of the cranial vault accompanied by absence of overlying tissues, including the brain and cerebral hemispheres, skull and scalp. Our Neurology team evaluates and manages anencephaly.
Classification
Ontology identifier: DOID:0060668 (Human Disease Ontology).
Classification path: physical disorder › congenital nervous system abnormality.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: Q00.0
- MeSH: D000757
- OMIM: 206500
Care at Weyland-Yutani Health System
Neurology specialists lead care for anencephaly. 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 anencephaly. Bring a list of current medications and any previous test results.
Reference links
Anterior spinal artery syndrome
A syndrome that is characterized by loss of function of the anterior two-thirds of the spinal cord that results from ischemia of the anterior spinal artery. Patients with anterior spinal artery syndrome are cared for through our Neurology service line.
Also known as
- Anterior spinal artery occlusion syndrome
Classification
Ontology identifier: DOID:6712 (Human Disease Ontology).
Classification path: syndrome.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G83.82
- MeSH: D020759
- SNOMED CT: 282785008
Care at Weyland-Yutani Health System
Neurology specialists lead care for anterior spinal artery syndrome. 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 anterior spinal artery syndrome, contact your primary care provider or schedule a visit with Neurology.
Reference links
Auditory system disease
auditory system disease: A sensory system disease that is characterized by auditory dysfunction located_in the auditory system.
Also known as
Classification
Ontology identifier: DOID:2742 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease.
Specialty: Neurology
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: H93.9
- ICD-9-CM: 388.9
- MeSH: D004427
- SNOMED CT: 194193002
Care at Weyland-Yutani Health System
Neurology specialists lead care for auditory system disease. 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 auditory system disease. Bring a list of current medications and any previous test results.
Reference links
Autosomal dominant nonsyndromic deafness
Overview. A nonsyndromic deafness characterized by an autosomal dominant inheritance mode. Weyland-Yutani Health System offers diagnosis and ongoing care for autosomal dominant nonsyndromic deafness.
Also known as
- autosomal dominant deafness
Classification
Ontology identifier: DOID:0050564 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease › nonsyndromic deafness.
Specialty: Neurology
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: H90.3
- OMIM: PS124900
Care at Weyland-Yutani Health System
Treatment of autosomal dominant nonsyndromic deafness 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 dominant nonsyndromic deafness, contact your primary care provider or schedule a visit with Neurology.
Reference links
Autosomal dominant nonsyndromic deafness 10
In clinical terms, autosomal dominant nonsyndromic deafness 10 is described as follows: an autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the third or forth decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the EYA4 gene on chromosome 6q23.
Also known as
- autosomal dominant deafness 10
- DFNA10
Classification
Ontology identifier: DOID:0110542 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease › nonsyndromic deafness › autosomal dominant nonsyndromic deafness.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H90.3
- OMIM: 601316
Care at Weyland-Yutani Health System
Care for autosomal dominant nonsyndromic deafness 10 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
If you or a family member may have autosomal dominant nonsyndromic deafness 10, contact your primary care provider or schedule a visit with Neurology.
Reference links
Autosomal dominant nonsyndromic deafness 12
An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and mid-frequency hearing loss and has_material_basis_in mutation in the TECTA gene on chromosome 11q23. This page summarizes how autosomal dominant nonsyndromic deafness 12 is classified and the care available at Weyland-Yutani Health System.
Also known as
- autosomal dominant deafness 12
- autosomal dominant deafness 8
- DFNA12
- DFNA8
Classification
Ontology identifier: DOID:0110544 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease › nonsyndromic deafness › autosomal dominant nonsyndromic deafness.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H90.3
- OMIM: 601543
Care at Weyland-Yutani Health System
Neurology specialists lead care for autosomal dominant nonsyndromic deafness 12. 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 autosomal dominant nonsyndromic deafness 12. Bring a list of current medications and any previous test results.
Reference links
Autosomal dominant nonsyndromic deafness 16
Overview. An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 2q23-q24.3. Weyland-Yutani Health System offers diagnosis and ongoing care for autosomal dominant nonsyndromic deafness 16.
Also known as
- autosomal dominant deafness 16
- DFNA16
Classification
Ontology identifier: DOID:0110547 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease › nonsyndromic deafness › autosomal dominant nonsyndromic deafness.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H90.3
- OMIM: 603964
Care at Weyland-Yutani Health System
Care for autosomal dominant nonsyndromic deafness 16 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 autosomal dominant nonsyndromic deafness 16? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Autosomal dominant nonsyndromic deafness 33
autosomal dominant nonsyndromic deafness 33: An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 13q34.
Also known as
- autosomal dominant deafness 33
- DFNA33
Classification
Ontology identifier: DOID:0110562 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease › nonsyndromic deafness › autosomal dominant nonsyndromic deafness.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H90.3
- OMIM: 614211
Care at Weyland-Yutani Health System
Neurology specialists lead care for autosomal dominant nonsyndromic deafness 33. 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 dominant nonsyndromic deafness 33, contact your primary care provider or schedule a visit with Neurology.
Reference links
Autosomal dominant nonsyndromic deafness 3A
autosomal dominant nonsyndromic deafness 3A: An autosomal dominant nonsyndromic deafness that is characterized by prelingual, high frequency hearing loss and has_material_basis_in mutation in the GJB2 gene on chromosome 13q12.
Also known as
- autosomal dominant deafness 3A
- DFNA3A
Classification
Ontology identifier: DOID:0110564 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease › nonsyndromic deafness › autosomal dominant nonsyndromic deafness.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H90.3
- OMIM: 601544
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, autosomal dominant nonsyndromic deafness 3A is managed by Neurology with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about autosomal dominant nonsyndromic deafness 3A? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Autosomal dominant nonsyndromic deafness 53
An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 14q11.2-q12. Patients with autosomal dominant nonsyndromic deafness 53 are cared for through our Neurology service line.
Also known as
- autosomal dominant deafness 53
- DFNA53
Classification
Ontology identifier: DOID:0110579 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › sensory system disease › auditory system disease › nonsyndromic deafness › autosomal dominant nonsyndromic deafness.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: H90.3
- OMIM: 609965
Care at Weyland-Yutani Health System
Care for autosomal dominant nonsyndromic deafness 53 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 autosomal dominant nonsyndromic deafness 53. Bring a list of current medications and any previous test results.
Reference links