Immunology and Allergy conditions, page 2 of 3
20 conditions on this page, alphabetically from Hypersensitivity reaction type IV disease to T cell deficiency. Each entry below describes the condition in full.
On this page
Hypersensitivity reaction type IV disease
A hypersensitivity reaction disease that is characterized by a cell-mediated response to antigens, where Th1 helper T cells react with antigens on antigen-presenting cells and cause a delayed type immune response. This page summarizes how hypersensitivity reaction type IV disease is classified and the care available at Weyland-Yutani Health System.
Classification
Ontology identifier: DOID:2916 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › hypersensitivity reaction disease.
Specialty: Immunology and Allergy
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: C88.90
- MeSH: D007160
- SNOMED CT: 127071007
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, hypersensitivity reaction type IV disease is managed by Immunology and Allergy 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 hypersensitivity reaction type IV disease, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links
Immune system disease
A disease of anatomical entity that is located_in the immune system. Patients with immune system disease are cared for through our Immunology and Allergy service line.
Classification
Ontology identifier: DOID:2914 (Human Disease Ontology).
Classification path: disease of anatomical entity.
Specialty: Immunology and Allergy
More specific conditions
Showing 25 of 31.
Medical codes
- ICD-10-CM: D89.9
- ICD-9-CM: 279.9
- SNOMED CT: 154782004
Care at Weyland-Yutani Health System
Immunology and Allergy specialists lead care for immune system disease. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about immune system disease? Call your nearest Weyland-Yutani location and ask for Immunology and Allergy.
Reference links
Immunodeficiency 52
immunodeficiency 52: A T cell deficiency characterized by onset of severe recurrent infections in infancy and a defect in T-cell receptor signaling resulting in variable immunological disorders that has_material_basis_in homozygous or compound heterozygous mutation in LAT on chromosome 16p11.2.
Also known as
- IMD52
- severe combined immunodeficiency due to LAT deficiency
Classification
Ontology identifier: DOID:0111983 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- OMIM: 617514
- SNOMED CT: 1179284005
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, immunodeficiency 52 is managed by Immunology and Allergy with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
When to seek care
Questions about immunodeficiency 52? Call your nearest Weyland-Yutani location and ask for Immunology and Allergy.
Reference links
Langerhans-cell histiocytosis
A histiocytosis that is characterized by clonal proliferation of Langerhans cells. Our Immunology and Allergy team evaluates and manages Langerhans-cell histiocytosis.
Also known as
- Histiocytosis X
- Langerhan's cell histiocytosis
- Langerhans cell granulomatosis
- Letterer-Siwe disease
- Letterer-Siwe disease involving intra-abdominal lymph nodes
- Letterer-Siwe disease involving intrapelvic lymph nodes
- Letterer-Siwe disease involving intrathoracic lymph nodes
- Letterer-Siwe disease involving lymph nodes of axilla and upper limb
- Letterer-Siwe disease involving lymph nodes of head, face and neck
- Letterer-Siwe disease involving lymph nodes of head, face, and neck
- Letterer-Siwe disease involving lymph nodes of inguinal region and lower limb
- Letterer-Siwe disease involving lymph nodes of multiple sites
- Letterer-Siwe disease involving spleen
- Letterer-Siwe disease of intra-abdominal lymph nodes
- Letterer-Siwe disease of intrapelvic lymph nodes
- Letterer-Siwe disease of intrathoracic lymph nodes
- Letterer-Siwe disease of lymph nodes of axilla and upper limb
- Letterer-Siwe disease of lymph nodes of axilla and/or upper limb
- Letterer-Siwe disease of lymph nodes of head, face and neck
- Letterer-Siwe disease of lymph nodes of head, face and/or neck
- Letterer-Siwe disease of lymph nodes of inguinal region amd/or lower limb
- Letterer-Siwe disease of lymph nodes of inguinal region and lower limb
- Letterer-Siwe disease of lymph nodes of inguinal region and/or lower limb
- Letterer-Siwe disease of lymph nodes of multiple sites
- Letterer-Siwe disease of spleen
Classification
Ontology identifier: DOID:2571 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › lymphatic system disease › histiocytosis.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: C96.0
- ICD-10-CM: C96.6
- ICD-9-CM: 202.5
- MeSH: D006646
- OMIM: 246400
- OMIM: 604856
- SNOMED CT: 154583006
- SNOMED CT: 234439008
Care at Weyland-Yutani Health System
Immunology and Allergy specialists lead care for Langerhans-cell histiocytosis. 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 Langerhans-cell histiocytosis. Bring a list of current medications and any previous test results.
Reference links
Lymphangitis
Overview. A lymphatic system disease that is characterized by inflammation of the lymphatic channels which occurs as a result of infection at a site distal to the channel. It is caused by Streptococcus pyogenes (Group A strep) or Staphylococcus aureus. Lymphangitis is also sometimes called blood poisoning. Weyland-Yutani Health System offers diagnosis and ongoing care for lymphangitis.
Classification
Ontology identifier: DOID:9317 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › lymphatic system disease.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: I89.1
- ICD-9-CM: 457.2
- MeSH: D008205
- SNOMED CT: 1415005
Care at Weyland-Yutani Health System
Treatment of lymphangitis begins with an evaluation in Immunology and Allergy. 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 lymphangitis, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links
Lymphatic system disease
An immune system disease that is located_in the lymphatic system. This page summarizes how lymphatic system disease is classified and the care available at Weyland-Yutani Health System.
Also known as
- disease of lympoid system
- disorder of lymph node and lymphatics
- disorder of lymphatic system
- disorder of lymphoid system
- Lymphangiopathy
- Lymphatic disease
- lymphatic disorder
- lympoid system disease
Classification
Ontology identifier: DOID:75 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease.
Specialty: Immunology and Allergy
Broader conditions
More specific conditions
Medical codes
- MeSH: D008206
- SNOMED CT: 266326002
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, lymphatic system disease is managed by Immunology and Allergy with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about lymphatic system disease? Call your nearest Weyland-Yutani location and ask for Immunology and Allergy.
Reference links
Lymphedema
In clinical terms, lymphedema is described as follows: A lymphatic system disease that is characterized by the abnormal accumulation of lymph fluid in the body's tissues, leading to swelling.
Also known as
- Lymphatic edema
- Lymphoedema
Classification
Ontology identifier: DOID:4977 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › lymphatic system disease.
Specialty: Immunology and Allergy
Broader conditions
More specific conditions
Medical codes
- MeSH: D008209
- SNOMED CT: 266334008
Care at Weyland-Yutani Health System
Immunology and Allergy specialists lead care for lymphedema. 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 lymphedema, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links
Lymphoproliferative syndrome 1
A lymphoproliferative syndrome characterized by autosomal recessive inheritance, early childhood onset of Epstein-Barr virus-associated immune dysregulation typically manifesting as lymphoma, lymphomatoid granulomatosis, hemophagocytic lymphohistiocytosis, Hodgkin disease, and-or hypogammaglobulinemia and that has_material_basis_in homozygous mutation in the ITK gene on chromosome 5q32. Patients with lymphoproliferative syndrome 1 are cared for through our Immunology and Allergy service line.
Also known as
Classification
Ontology identifier: DOID:0060707 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: D47.9
- OMIM: 613011
Care at Weyland-Yutani Health System
Care for lymphoproliferative syndrome 1 is coordinated through Immunology and Allergy. 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 lymphoproliferative syndrome 1, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links
MHC class II deficiency
MHC class II deficiency: A severe combined immunodeficiency that is characterized by deficiency of MHC class II molecules that causes lack of immune protection against bacteria, viruses, and fungi and thus causes early death in childhood, and has_material_basis_in autosomal recessive inheritance of mutation in the CIITA, RFX5, RFXANK, and RFXAP genes.
Also known as
- bare lymphocyte syndrome type II
- BLSII
- SCID due to absent class II HLA antigens
Classification
Ontology identifier: DOID:5812 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › primary immunodeficiency disease › combined immunodeficiency › severe combined immunodeficiency.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: D81.6
- MeSH: D016511
- OMIM: 209920
- SNOMED CT: 71904008
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, MHC class II deficiency is managed by Immunology and Allergy 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 MHC class II deficiency, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links
Mikulicz disease
Mikulicz disease: An autoimmune disease that is characterized by chronic enlargement of the glands of the head and neck, has_symptom lumps of the face and neck, dry eyes, dry mouth, and intermittent fever, and is often associated with an underlying autoimmune disorder, hematologic malignancy, tuberculosis infection, or syphilis infection.
Also known as
- IgG4-related dacryoadenitis and sialadenitis
- Mikulicz's disease
Classification
Ontology identifier: DOID:12900 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › autoimmune disease.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: K11.8
- MeSH: D008882
- SNOMED CT: 7826003
Care at Weyland-Yutani Health System
Treatment of Mikulicz disease begins with an evaluation in Immunology and Allergy. 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 Mikulicz disease. Bring a list of current medications and any previous test results.
Reference links
Multiple sclerosis
multiple sclerosis: A demyelinating disease that involves damage to the fatty myelin sheaths around the axons of the brain and spinal cord resulting in demyelination and scarring.
Also known as
- Generalized multiple sclerosis
- insular sclerosis
Classification
Ontology identifier: DOID:2377 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › autoimmune disease of central nervous system.
Specialty: Immunology and Allergy
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: G35
- ICD-9-CM: 340
- MeSH: D009103
- OMIM: 612594
- OMIM: 612595
- OMIM: 612596
- SNOMED CT: 155023009
Care at Weyland-Yutani Health System
Care for multiple sclerosis is coordinated through Immunology and Allergy. 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 multiple sclerosis, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links
Neuromyelitis optica
In clinical terms, neuromyelitis optica is described as follows: A central nervous system disease characterized by inflammation of the optic nerve (optic neuritis) and inflammation of the spinal cord (myelitis).
Also known as
- Devic's disease
- Devic's syndrome
Classification
Ontology identifier: DOID:8869 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › autoimmune disease of central nervous system.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: G36.0
- ICD-9-CM: 341.0
- MeSH: D009471
- SNOMED CT: 25044007
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, neuromyelitis optica is managed by Immunology and Allergy 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 neuromyelitis optica, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links
Primary immunodeficiency disease
In clinical terms, primary immunodeficiency disease is described as follows: an immune system disease that results when one or more essential parts of the immune system is missing or not working properly at birth due to a genetic mutation.
Also known as
- hypoimmunity
- immune deficiency disorder
- immunodeficiency syndrome
Classification
Ontology identifier: DOID:612 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease.
Specialty: Immunology and Allergy
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: D84.9
- ICD-9-CM: 279.3
- MeSH: D007153
- OMIM: 242850
- OMIM: PS300755
- SNOMED CT: 191005003
Care at Weyland-Yutani Health System
Immunology and Allergy specialists lead care for primary immunodeficiency 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 primary immunodeficiency disease, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links
Progressive relapsing multiple sclerosis
A multiple sclerosis that is characterized by steadily worsening symptoms and attacks during periods of remission with disease progression from the onset. Patients with progressive relapsing multiple sclerosis are cared for through our Immunology and Allergy service line.
Also known as
- PRMS
- Progressive-relapsing MS
Classification
Ontology identifier: DOID:0050785 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › autoimmune disease of central nervous system › multiple sclerosis.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- MeSH: D020528
- SNOMED CT: 724778008
Care at Weyland-Yutani Health System
Treatment of progressive relapsing multiple sclerosis begins with an evaluation in Immunology and Allergy. 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 progressive relapsing multiple sclerosis, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links
Relapsing-remitting multiple sclerosis
A multiple sclerosis that is characterized by relapse (attacks of symptom flare-ups) followed by remission (periods of recovery). Symptoms may vary from mild to severe, and relapses and remissions may last for days or months. More than 80 percent of people who have MS begin with relapsing-remitting cycles. This page summarizes how relapsing-remitting multiple sclerosis is classified and the care available at Weyland-Yutani Health System.
Also known as
- Relapsing-remitting MS
- RRMS
Classification
Ontology identifier: DOID:2378 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › autoimmune disease of central nervous system › multiple sclerosis.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: G35.A
- MeSH: D020529
- SNOMED CT: 426373005
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, relapsing-remitting multiple sclerosis is managed by Immunology and Allergy 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 relapsing-remitting multiple sclerosis, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links
Secondary progressive multiple sclerosis
A multiple sclerosis that is characterized by a worsening of disability, rather than by relapses followed by recovery, which progressively worsens until a steady progression of disability replaces the cycles of attacks. Our Immunology and Allergy team evaluates and manages secondary progressive multiple sclerosis.
Also known as
- Secondary-progressive MS
- SPMS
Classification
Ontology identifier: DOID:0050783 (Human Disease Ontology).
Classification path: disease of anatomical entity › nervous system disease › central nervous system disease › autoimmune disease of central nervous system › multiple sclerosis.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: G35.C
- MeSH: D020528
- SNOMED CT: 425500002
Care at Weyland-Yutani Health System
Care for secondary progressive multiple sclerosis is coordinated through Immunology and Allergy. 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 secondary progressive multiple sclerosis, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links
Selective IgA deficiency disease
In clinical terms, selective IgA deficiency disease is described as follows: A selective immunoglobulin deficiency disease that is the result of a deficiency of immunoglobulin A (IgA), an antibody that protects against infections of the mucous membranes lining the mouth, airways, and digestive tract.
Also known as
- Immunoglobulin A deficiency
- selective IgA immunodeficiency
- Selective immunoglobulin A deficiency
Classification
Ontology identifier: DOID:11701 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › primary immunodeficiency disease › B cell deficiency › selective immunoglobulin deficiency disease › dysgammaglobulinemia.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- MeSH: D017098
- SNOMED CT: 29260007
Care at Weyland-Yutani Health System
Immunology and Allergy specialists lead care for selective IgA deficiency 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 selective IgA deficiency disease, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links
Selective IgD deficiency disease
Overview. A selective immunoglobulin deficiency disease that is characterized by low serum levels of IgD immunoglobulins, but is associated with few clinical symptoms. Weyland-Yutani Health System offers diagnosis and ongoing care for selective IgD deficiency disease.
Also known as
- Selective IgD Immunodeficiency
- Selective immunoglobulin D deficiency
Classification
Ontology identifier: DOID:7263 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › primary immunodeficiency disease › B cell deficiency › selective immunoglobulin deficiency disease.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
Care at Weyland-Yutani Health System
Care for selective IgD deficiency disease is coordinated through Immunology and Allergy. 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 selective IgD deficiency disease. Bring a list of current medications and any previous test results.
Reference links
Severe combined immunodeficiency
severe combined immunodeficiency: A combined T cell and B cell immunodeficiency that is caused by a defect in infection-fighting immune cells resulting in individuals with non-functional immune systems.
Also known as
- combined T and B cell inborn immunodeficiency
- SCID
Classification
Ontology identifier: DOID:627 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › primary immunodeficiency disease › combined immunodeficiency.
Specialty: Immunology and Allergy
Broader conditions
More specific conditions
Medical codes
- MeSH: D016511
- SNOMED CT: 190994004
Care at Weyland-Yutani Health System
Immunology and Allergy specialists lead care for severe combined immunodeficiency. 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 severe combined immunodeficiency, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links
T cell deficiency
In clinical terms, T cell deficiency is described as follows: A primary immunodeficiency disease that is characterized by decreased numbers of circulating or functioning T cells.
Also known as
- T cell immunodeficiency
- T lymphocyte deficiency
- T lymphocyte immunodeficiency
Classification
Ontology identifier: DOID:11200 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › primary immunodeficiency disease.
Specialty: Immunology and Allergy
Broader conditions
More specific conditions
Medical codes
Care at Weyland-Yutani Health System
Immunology and Allergy specialists lead care for T cell deficiency. 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 T cell deficiency, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links