Neurology conditions, page 4 of 6
20 conditions on this page, alphabetically from Hereditary spastic paraplegia 54 to Migraine. Each entry below describes the condition in full.
On this page
Hereditary spastic paraplegia 54
A hereditary spastic paraplegia that has_material_basis_in mutation in the DDHD2 gene on chromosome 8p11. Our Neurology team evaluates and manages hereditary spastic paraplegia 54.
Also known as
- autosomal recessive spastic paraplegia 54
- autosomal recessive spastic paraplegia type 54
- SPG54
Classification
Ontology identifier: DOID:0110806 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G11.4
- OMIM: 615033
Care at Weyland-Yutani Health System
Treatment of hereditary spastic paraplegia 54 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 hereditary spastic paraplegia 54, contact your primary care provider or schedule a visit with Neurology.
Reference links
Hereditary spastic paraplegia 64
In clinical terms, hereditary spastic paraplegia 64 is described as follows: A hereditary spastic paraplegia that has_material_basis_in mutation in the ENTPD1 gene on chromosome 10q24.
Also known as
- autosomal recessive spastic paraplegia 64
- autosomal recessive spastic paraplegia type 64
- SPG64
Classification
Ontology identifier: DOID:0110815 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G11.4
- OMIM: 615683
Care at Weyland-Yutani Health System
Treatment of hereditary spastic paraplegia 64 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 hereditary spastic paraplegia 64, contact your primary care provider or schedule a visit with Neurology.
Reference links
Hypoglossal nerve disease
Overview. A glossopharyngeal nerve disease that is located_in the hypoglossal nerve (twelfth cranial nerve). Weyland-Yutani Health System offers diagnosis and ongoing care for hypoglossal nerve disease.
Also known as
- disorder of 12th nerve
- disorder of hypoglossal [12th] nerve
- disorder of hypoglossal nerve
- disorder of XII nerve
Classification
Ontology identifier: DOID:13814 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › peripheral nervous system disease › neuropathy › cranial nerve disease › glossopharyngeal nerve disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G52.3
- ICD-9-CM: 352.5
- MeSH: D020437
- SNOMED CT: 24777009
Care at Weyland-Yutani Health System
Care for hypoglossal nerve 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 hypoglossal nerve disease. Bring a list of current medications and any previous test results.
Reference links
Hypomyelinating leukodystrophy 11
hypomyelinating leukodystrophy 11: A hypomyelinating leukodystrophy characterized by autosomal recessive inheritance of delayed psychomotor development and other neurologic features associated with hypomyelination that has_material_basis_in homozygous or compound heterozygous mutation in the POLR1C gene on chromosome 6p21.
Also known as
Classification
Ontology identifier: DOID:0060792 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G11.1
- OMIM: 616494
Care at Weyland-Yutani Health System
Neurology specialists lead care for hypomyelinating leukodystrophy 11. 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 hypomyelinating leukodystrophy 11. Bring a list of current medications and any previous test results.
Reference links
Inflammatory and toxic neuropathy
inflammatory and toxic neuropathy: A neuropathy that is caused by drug ingestion, drug or chemical abuse, or industrial chemical exposure from the workplace or the environment.
Classification
Ontology identifier: DOID:2537 (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: 357
- SNOMED CT: 193172009
Care at Weyland-Yutani Health System
Care for inflammatory and toxic 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
If you or a family member may have inflammatory and toxic neuropathy, contact your primary care provider or schedule a visit with Neurology.
Reference links
Intermediate spinal muscular atrophy
A childhood spinal muscular atrophy that is characterized by progressive muscular weakness and respiratory failure, develops in children between the ages of 6 and 12 months and drastically reduces length of life, and has_material_basis_in mutations in the SMN1 or SMN2 genes that are required for the survival of motor neurons. Our Neurology team evaluates and manages intermediate spinal muscular atrophy.
Also known as
- MUSCULAR ATROPHY, SPINAL, INFANTILE CHRONIC FORM
- MUSCULAR ATROPHY, SPINAL, INTERMEDIATE TYPE
- SMA II
- SMA2
- spinal muscular atrophy 2
- spinal muscular atrophy type II
Classification
Ontology identifier: DOID:0050530 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease.
Specialty: Neurology
Broader conditions
Medical codes
- MeSH: D014897
- OMIM: 253550
- SNOMED CT: 128212001
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, intermediate spinal muscular atrophy is managed by Neurology 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 intermediate spinal muscular atrophy. Bring a list of current medications and any previous test results.
Reference links
Intracranial abscess
A central nervous system disease that is located_in the skull and is characterized by a collection of pus (infected material) inside the skull. Patients with intracranial abscess are cared for through our Neurology service line.
Classification
Ontology identifier: DOID:10095 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-9-CM: 324.0
- SNOMED CT: 192738001
Care at Weyland-Yutani Health System
Neurology specialists lead care for intracranial abscess. 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 intracranial abscess, contact your primary care provider or schedule a visit with Neurology.
Reference links
Intracranial hypertension
A brain disease that is characterized by high pressure inside the skull, the brain tissue and cerebrospinal fluid, has_symptom headache, has_symptom vomiting, has_symptom altered mental status, has_symptom papilledema. This page summarizes how intracranial hypertension is classified and the care available at Weyland-Yutani Health System.
Also known as
- Raised intracranial pressure
Classification
Ontology identifier: DOID:9428 (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: D019586
- SNOMED CT: 155052007
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, intracranial hypertension 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 intracranial hypertension, contact your primary care provider or schedule a visit with Neurology.
Reference links
Intracranial hypotension
A brain disease that is characterized by low pressure inside the skull, and thus in the brain tissue and cerebrospinal fluid; may occur as a result of an occult or iatrogenically caused leak of CSF into another body cavity; may result in the downward displacement of the cerebellar tonsils through the foramen magnum or Chiari malformation; has_symptom orthostatic headache; other symptoms are related to compression of cranial nerves due to brain sagging. This page summarizes how intracranial hypotension is classified and the care available at Weyland-Yutani Health System.
Classification
Ontology identifier: DOID:4723 (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: G96.81
- MeSH: D019585
- SNOMED CT: 433691000124104
Care at Weyland-Yutani Health System
Treatment of intracranial hypotension 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 intracranial hypotension. Bring a list of current medications and any previous test results.
Reference links
Jaw-winking syndrome
A cranial nerve disease characterized by unilateral congenital ptosis and rapid exaggerated elevation of the ptotic lid on moving of the lower jaw. Patients with jaw-winking syndrome are cared for through our Neurology service line.
Also known as
- abnormal innervation syndrome of eyelid
- Jaw-blinking
- Marcus-Gunn syndrome
- Pterygoid-levator synkinesis
Classification
Ontology identifier: DOID:560 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › peripheral nervous system disease › neuropathy › cranial nerve disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: Q07.8
- ICD-9-CM: 374.43
- MeSH: C535908
- OMIM: 154600
- SNOMED CT: 5127009
Care at Weyland-Yutani Health System
Care for jaw-winking syndrome 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 jaw-winking syndrome, contact your primary care provider or schedule a visit with Neurology.
Reference links
Joubert syndrome
A ciliopathy that is characterized by congenital malformation of the brainstem and agenesis or hypoplasia of the cerebellar vermis leading to an abnormal respiratory pattern, nystagmus, hypotonia, ataxia, and delay in achieving motor milestones. This page summarizes how Joubert syndrome is classified and the care available at Weyland-Yutani Health System.
Also known as
Classification
Ontology identifier: DOID:0050777 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › ciliopathy.
Specialty: Neurology
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: Q04.3
- OMIM: PS213300
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, Joubert syndrome 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 Joubert syndrome, contact your primary care provider or schedule a visit with Neurology.
Reference links
Joubert syndrome with orofaciodigital defect
A Joubert syndrome that is characterized by orofaciodigital defect. This page summarizes how Joubert syndrome with orofaciodigital defect is classified and the care available at Weyland-Yutani Health System.
Also known as
- OFD6
- orofaciodigital syndrome VI
- Polydactyly cleft lip palate psychomotor retardation
- Varadi syndrome
- Varadi-Papp syndrome
Classification
Ontology identifier: DOID:0060376 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › ciliopathy › Joubert syndrome.
Specialty: Neurology
Broader conditions
Medical codes
- MeSH: C536531
- OMIM: 277170
- SNOMED CT: 721873007
Care at Weyland-Yutani Health System
Neurology specialists lead care for Joubert syndrome with orofaciodigital defect. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Questions about Joubert syndrome with orofaciodigital defect? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Lafora disease
A progressive myoclonus epilepsy characterized by myoclonus and/or generalized seizures, visual hallucinations, and progressive neurological decline with onset between 8 and 18 years of age that has_material_basis_in homozygous or compound heterozygous mutation in either NHLRC1 on chromosome 6p22.3 or EPM2A on chromosome 6q24.3. Our Neurology team evaluates and manages Lafora disease.
Also known as
- Lafora Progressive Myoclonic Epilepsy
- Lafora's disease
- MYOCLONIC EPILEPSY OF LAFORA
- progressive myoclonic epilepsy 2
Classification
Ontology identifier: DOID:3534 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G40.C
- MeSH: D020192
- OMIM: PS254780
- SNOMED CT: 230425004
Care at Weyland-Yutani Health System
Neurology specialists lead care for Lafora 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 Lafora disease, contact your primary care provider or schedule a visit with Neurology.
Reference links
Leukodystrophy
Overview. A cerebral degeneration characterized by dysfunction of the white matter of the brain. Weyland-Yutani Health System offers diagnosis and ongoing care for leukodystrophy.
Classification
Ontology identifier: DOID:10579 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › brain disease › cerebral degeneration.
Specialty: Neurology
Broader conditions
More specific conditions
Medical codes
- ICD-9-CM: 330.0
- SNOMED CT: 5101009
Care at Weyland-Yutani Health System
Neurology specialists lead care for leukodystrophy. 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 leukodystrophy. Bring a list of current medications and any previous test results.
Reference links
Lissencephaly
lissencephaly: A congenital nervous system abnormality characterized by the absence of folds in the cerebral cortex and caused_by defective neuronal migration during the 12th to 24th weeks of gestation.
Classification
Ontology identifier: DOID:0050453 (Human Disease Ontology).
Classification path: physical disorder › congenital nervous system abnormality.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: Q04.3
- MeSH: D054082
- OMIM: PS607432
- SNOMED CT: 204036008
- SNOMED CT: 23024003
Care at Weyland-Yutani Health System
Treatment of lissencephaly 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 lissencephaly, contact your primary care provider or schedule a visit with Neurology.
Reference links
Machado-Joseph disease
An autosomal dominant cerebellar ataxia that is characterized by slow degeneration of the hindbrain and has_material_basis_in expansion of CAG triplet repeats (glutamine) in the ATXN3 gene. Our Neurology team evaluates and manages Machado-Joseph disease.
Also known as
- Azorean disease
- MJD
- SCA3
- spinocerebellar ataxia 3
- spinocerebellar ataxia type 3
Classification
Ontology identifier: DOID:1440 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal dominant disease › autosomal dominant cerebellar ataxia.
Specialty: Neurology
Broader conditions
Medical codes
- MeSH: D017827
- OMIM: 109150
- SNOMED CT: 91952008
Care at Weyland-Yutani Health System
Care for Machado-Joseph disease 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 Machado-Joseph disease, contact your primary care provider or schedule a visit with Neurology.
Reference links
Mast syndrome
A hereditary spastic paraplegia associated with dementia. Patients with Mast syndrome are cared for through our Neurology service line.
Also known as
- autosomal recessive spastic paraplegia 21
- autosomal recessive spastic paraplegia type 21
- hereditary spastic paraplegia 21
- SPG21
Classification
Ontology identifier: DOID:0060245 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › paraplegia › hereditary spastic paraplegia.
Specialty: Neurology
Broader conditions
Medical codes
- ICD-10-CM: G11.4
- MeSH: C565409
- OMIM: 248900
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, Mast syndrome is managed by Neurology 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 Mast syndrome, contact your primary care provider or schedule a visit with Neurology.
Reference links
Meningitis
meningitis: A central nervous system disease that is characterized by an inflammation of the pia-arachnoid meninges. It can be caused by growth of bacteria, fungi, or parasites within the subarachnoid space or by the growth of bacteria or viruses within the meningeal or ependymal cells.
Classification
Ontology identifier: DOID:9471 (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: G03
- ICD-9-CM: 322.9
- MeSH: D008581
- SNOMED CT: 154983000
Care at Weyland-Yutani Health System
Treatment of meningitis 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 meningitis? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Meningoencephalitis
A central nervous system disease that involves encephalitis which occurs along with meningitis. Patients with meningoencephalitis are cared for through our Neurology service line.
Classification
Ontology identifier: DOID:10554 (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: A69.22
- MeSH: D008590
- SNOMED CT: 7125002
Care at Weyland-Yutani Health System
Treatment of meningoencephalitis 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 meningoencephalitis? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links
Migraine
A brain disease that is characterized by moderate to severe headaches, nausea, extreme sensitivity to light and sound and intense unilaterial throbbing or pulsing. Our Neurology team evaluates and manages migraine.
Also known as
- migraine disorder
- migraine variant
- migraine with or without aura
Classification
Ontology identifier: DOID:6364 (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
- ICD-10-CM: G43
- ICD-9-CM: 346
- MeSH: D008881
- OMIM: 157300
- SNOMED CT: 155046006
- SNOMED CT: 193036004
Care at Weyland-Yutani Health System
Treatment of migraine 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 migraine? Call your nearest Weyland-Yutani location and ask for Neurology.
Reference links