Immunology and Allergy conditions, page 1 of 3
20 conditions on this page, alphabetically from Adenosine deaminase deficiency to Hirata disease. Each entry below describes the condition in full.
On this page
Adenosine deaminase deficiency
A severe combined immunodeficiency that is caused by a defective enzyme, adenosine deaminase (ADA), necessary for the breakdown of purines. Lack of ADA causes accumulation of dATP. Patients with adenosine deaminase deficiency are cared for through our Immunology and Allergy service line.
Also known as
Classification
Ontology identifier: DOID:5810 (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: D81.30
- OMIM: 102700
- SNOMED CT: 190999009
Care at Weyland-Yutani Health System
Treatment of adenosine deaminase deficiency 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
Questions about adenosine deaminase deficiency? Call your nearest Weyland-Yutani location and ask for Immunology and Allergy.
Reference links
Agammaglobulinemia
Overview. A B cell deficiency that is caused by a reduction in all types of gamma globulins. Weyland-Yutani Health System offers diagnosis and ongoing care for agammaglobulinemia.
Also known as
- hypogammaglobulinemia
- IGHM
- mu heavy chain deficiency
Classification
Ontology identifier: DOID:2583 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease.
Specialty: Immunology and Allergy
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: D80.1
- ICD-9-CM: 279.00
- MeSH: D000361
- OMIM: PS601495
- SNOMED CT: 119250001
- SNOMED CT: 267512002
Care at Weyland-Yutani Health System
Care for agammaglobulinemia 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 agammaglobulinemia, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links
Arthus reaction
A hypersensitivity reaction type III disease that is characterized by local vasculitis, has_symptom pain, edema, hemorrhage, or necrosis, and has_material_basis_in deposition of antigen-antibody immune complexes in vascular or serosal walls. Our Immunology and Allergy team evaluates and manages arthus reaction.
Also known as
- Arthus phenomenon
- Arthus type urticaria
Classification
Ontology identifier: DOID:1556 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › hypersensitivity reaction disease › hypersensitivity reaction type III disease.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: T78.41
- ICD-9-CM: 995.21
- MeSH: D001183
- SNOMED CT: 402413008
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, arthus reaction 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 arthus reaction? Call your nearest Weyland-Yutani location and ask for Immunology and Allergy.
Reference links
Autoimmune lymphoproliferative syndrome type 2A
Overview. An autoimmune lymphoproliferative syndrome that has_material_basis_in mutation in the CASP10 gene. Weyland-Yutani Health System offers diagnosis and ongoing care for autoimmune lymphoproliferative syndrome type 2A.
Also known as
- ALPS2A
- autoimmune lymphoproliferative syndrome type IIA
Classification
Ontology identifier: DOID:0110115 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal dominant disease.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: D47.9
- MeSH: C565833
- OMIM: 603909
Care at Weyland-Yutani Health System
Treatment of autoimmune lymphoproliferative syndrome type 2A 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
Questions about autoimmune lymphoproliferative syndrome type 2A? Call your nearest Weyland-Yutani location and ask for Immunology and Allergy.
Reference links
Autoimmune polyendocrine syndrome
An autoimmune disease of endocrine system characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs. Patients with autoimmune polyendocrine syndrome are cared for through our Immunology and Allergy service line.
Also known as
- autoimmune polyendocrinopathy
- Autoimmune polyglandular failure
- Lloyd's syndrome
Classification
Ontology identifier: DOID:14040 (Human Disease Ontology).
Classification path: disease of anatomical entity › endocrine system disease › autoimmune disease of endocrine system.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: E31.0
- MeSH: D016884
- SNOMED CT: 41864002
Care at Weyland-Yutani Health System
Immunology and Allergy specialists lead care for autoimmune polyendocrine syndrome. 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 autoimmune polyendocrine syndrome. Bring a list of current medications and any previous test results.
Reference links
Autoimmune thyroiditis
An autoimmune disease of endocrine system that involves inflammation located_in thyroid gland caused by the immune system reacting against its own tissues. This page summarizes how autoimmune thyroiditis is classified and the care available at Weyland-Yutani Health System.
Also known as
- Chronic Lymphocytic Thyroiditis
- Hashimoto thyroiditis
- Hashimoto's Disease
- Hashimoto's syndrome
- Hashimoto's thyroiditis
- Lymphocytic Thyroiditis
Classification
Ontology identifier: DOID:7188 (Human Disease Ontology).
Classification path: disease of anatomical entity › endocrine system disease › autoimmune disease of endocrine system.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: E06.3
- MeSH: D013967
- SNOMED CT: 190297000
Care at Weyland-Yutani Health System
Treatment of autoimmune thyroiditis 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
Questions about autoimmune thyroiditis? Call your nearest Weyland-Yutani location and ask for Immunology and Allergy.
Reference links
B cell deficiency
A primary immunnodeficiency disease that is caused by a lack of infection-fighting antibody producing B cells (immunoglobulins) or B cells that are not functioning properly. Patients with B cell deficiency are cared for through our Immunology and Allergy service line.
Also known as
- B cell (antibody) deficiencies
- Immunoglobulin heavy chain deficiency
- immunoglobulin heavy chain deletion
Classification
Ontology identifier: DOID:2115 (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
- ICD-9-CM: 279.03
- SNOMED CT: 190982008
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, B cell deficiency 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 B cell deficiency, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links
Cardiac sarcoidosis
cardiac sarcoidosis: A sarcoidosis that is characterized by conduction abnormalities, arrhythmias, and congestive heart failure with noncaseating granulomas present on endomyocardial biopsy, and develops_from a type IV hypersensitivity reaction with noncaseating granulomas infiltrating the myocardial tissue, especially that of the left ventricle.
Classification
Ontology identifier: DOID:13405 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › hypersensitivity reaction disease › hypersensitivity reaction type IV disease › sarcoidosis.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, cardiac sarcoidosis is managed by Immunology and Allergy 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 cardiac sarcoidosis. Bring a list of current medications and any previous test results.
Reference links
Chronic granulomatous disease
Overview. A phagocyte bactericidal dysfunction characterized by an inability to resist repeated infectious diseases and a tendency to develop chronic inflammation. Life-threatening recurrent fungal and bacterial infections affecting the skin, lungs, liver, lymph nodes, and bones may occur along with swollen areas of inflamed tissues known as granulomas that can be widely distributed. Weyland-Yutani Health System offers diagnosis and ongoing care for chronic granulomatous disease.
Also known as
- Bridges-Good syndrome
- CGD
- Congenital dysphagocytosis
- Quie syndrome
Classification
Ontology identifier: DOID:3265 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › primary immunodeficiency disease › phagocyte bactericidal dysfunction.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: D71.8
- MeSH: D006105
- OMIM: PS306400
- SNOMED CT: 11210002
Care at Weyland-Yutani Health System
Treatment of chronic granulomatous 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
Questions about chronic granulomatous disease? Call your nearest Weyland-Yutani location and ask for Immunology and Allergy.
Reference links
Chronic NK-cell lymphocytosis
A hypersensitivity reaction type IV disease that is characterized by absolute lymphocytosis of natural killer (CD3- CD16+) cells often with concurrent cytopenia and has_symptom fever, arthralgia, apthous ulcers, vasculitic skin rash, and peripheral neuropathy. Our Immunology and Allergy team evaluates and manages chronic NK-cell lymphocytosis.
Also known as
- NK-cell large granular Lymphocyte Lymphocytosis
Classification
Ontology identifier: DOID:7465 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › hypersensitivity reaction disease › hypersensitivity reaction type IV disease.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
Care at Weyland-Yutani Health System
Immunology and Allergy specialists lead care for chronic NK-cell lymphocytosis. 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 chronic NK-cell lymphocytosis. Bring a list of current medications and any previous test results.
Reference links
Common variable immunodeficiency
An agammaglobulinemia that is characterized by low Ig levels with phenotypically normal B cells that can proliferate but do not develop into Ig-producing cells and that results in insufficient production of antibodies needed to respond to exposure of pathogens. Our Immunology and Allergy team evaluates and manages common variable immunodeficiency.
Also known as
- acquired agammaglobulinemia
- acquired hypogammaglobulinemia
- common variable agammaglobulinemia
- CVID
- sporadic hypogammaglobulinemia
Classification
Ontology identifier: DOID:12177 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › agammaglobulinemia.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: D83
- ICD-9-CM: 279.06
- MeSH: D017074
- OMIM: PS607594
- SNOMED CT: 23238000
Care at Weyland-Yutani Health System
Immunology and Allergy specialists lead care for common variable immunodeficiency. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about common variable immunodeficiency? Call your nearest Weyland-Yutani location and ask for Immunology and Allergy.
Reference links
Complement deficiency
In clinical terms, complement deficiency is described as follows: A primary immunodeficiency disease that is the result in a mutation of a gene encoding one of the thirty complement system proteins, produced predominantly in liver, which function to defend against infection and produce inflammation.
Also known as
- Complement deficiency disease
Classification
Ontology identifier: DOID:626 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › primary immunodeficiency disease.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: D84.1
- MeSH: D000081208
- SNOMED CT: 191014008
Care at Weyland-Yutani Health System
Care for complement deficiency 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 complement deficiency. Bring a list of current medications and any previous test results.
Reference links
Egg allergy
Overview. A food allergy that is an allergy or hypersensitivity to dietary substances from the yolk or whites of eggs, causing an overreaction of the immune system which may lead to severe physical symptoms. Weyland-Yutani Health System offers diagnosis and ongoing care for egg allergy.
Also known as
Classification
Ontology identifier: DOID:4377 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › allergic disease › gastrointestinal allergy › food allergy.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- MeSH: D021181
- SNOMED CT: 213019003
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, egg allergy is managed by Immunology and Allergy 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 egg allergy. Bring a list of current medications and any previous test results.
Reference links
Elephantiasis
Overview. A lymphedema that is characterised by edema, hypertrophy, and fibrosis of skin and subcutaneous tissues, due to obstruction of lymphatic vessels resulting in the enlargement and hardening of limbs or body parts due to tissue swelling (edema). Weyland-Yutani Health System offers diagnosis and ongoing care for elephantiasis.
Classification
Ontology identifier: DOID:4976 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › lymphatic system disease › lymphedema.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- MeSH: D004604
- SNOMED CT: 155485008
Care at Weyland-Yutani Health System
Care for elephantiasis 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
Questions about elephantiasis? Call your nearest Weyland-Yutani location and ask for Immunology and Allergy.
Reference links
Familial cold autoinflammatory syndrome 4
A familial cold autoinflammatory syndrome that is characterized by episodic high fevers, urticaria-like rash, and arthralgias starting at 2-3 months of age and often induced by cold-exposure that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the NLRC4 gene on chromosome 2p22. This page summarizes how familial cold autoinflammatory syndrome 4 is classified and the care available at Weyland-Yutani Health System.
Also known as
Classification
Ontology identifier: DOID:0090065 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal dominant disease.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: L50.2
- OMIM: 616115
Care at Weyland-Yutani Health System
Immunology and Allergy specialists lead care for familial cold autoinflammatory syndrome 4. 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 familial cold autoinflammatory syndrome 4. Bring a list of current medications and any previous test results.
Reference links
Graves' disease
Overview. An autoimmune disease of endocrine system that involves production of excessive amount of thyroid hormones, located_in thyroid gland. Weyland-Yutani Health System offers diagnosis and ongoing care for Graves' disease.
Also known as
- exophthalmic goiter
- Grave's disease
- Graves disease
Classification
Ontology identifier: DOID:12361 (Human Disease Ontology).
Classification path: disease of anatomical entity › endocrine system disease › autoimmune disease of endocrine system.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: E05.0
- MeSH: D006111
- OMIM: 275000
- SNOMED CT: 154655004
Care at Weyland-Yutani Health System
Immunology and Allergy specialists lead care for Graves' disease. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Questions about Graves' disease? Call your nearest Weyland-Yutani location and ask for Immunology and Allergy.
Reference links
Heavy chain disease
Overview. A hypersensitivity reaction type IV disease that results from a proliferation of cells producing immunoglobulin heavy chains. Weyland-Yutani Health System offers diagnosis and ongoing care for heavy chain disease.
Classification
Ontology identifier: DOID:0060125 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › hypersensitivity reaction disease › hypersensitivity reaction type IV disease.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- ICD-10-CM: C88.2
- MeSH: D006362
- SNOMED CT: 61493004
- SNOMED CT: 6381009
- SNOMED CT: 68979007
Care at Weyland-Yutani Health System
Immunology and Allergy specialists lead care for heavy chain 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 heavy chain disease, contact your primary care provider or schedule a visit with Immunology and Allergy.
Reference links
Hemophagocytic lymphohistiocytosis
A lymphatic system disease that is characterized by an expansion of the monocyte-macrophage population and intense hemophagocytosis. It can occur de novo, but more often occurs in the setting of another disorder, usually an infection or a malignancy. A clinical picture of fever, hepatosplenomegaly, lymphadenopathy and peripheral pancytopenia. The morphologic hallmark of this syndrome is the phagocytosis of hematopoietic elements by morphologically normal macrophages. This page summarizes how hemophagocytic lymphohistiocytosis is classified and the care available at Weyland-Yutani Health System.
Also known as
Classification
Ontology identifier: DOID:0050120 (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: D76.1
- MeSH: D051359
- OMIM: PS267700
- SNOMED CT: 190958003
Care at Weyland-Yutani Health System
Immunology and Allergy specialists lead care for hemophagocytic lymphohistiocytosis. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Questions about hemophagocytic lymphohistiocytosis? Call your nearest Weyland-Yutani location and ask for Immunology and Allergy.
Reference links
Hennekam syndrome
In clinical terms, Hennekam syndrome is described as follows: A lymphatic system disease characterized by he presence of intestinal lymphangiectasia, mental retardation, and characteristic facial anomalies. It is inherited in an autosomal recessive pattern. Most individuals with Hennekam syndrome have characteristic facial abnormalities, such as a flat face with accompanying puffy eyelids and hypertelorism; the nasal bridge is typically flat and the ears are typically small. Congenital extremity and genital lymphedema is present in most patients.
Also known as
- Hennekam lymphangiectasia-lymphedema syndrome
- lymphedem-lymphangiectasia-intellectual disability syndrome
Classification
Ontology identifier: DOID:0060366 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › lymphatic system disease.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
- MeSH: C537255
- OMIM: 235510
- OMIM: 616006
- SNOMED CT: 234146006
Care at Weyland-Yutani Health System
Treatment of Hennekam syndrome 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
Seek a medical evaluation if you are concerned about Hennekam syndrome. Bring a list of current medications and any previous test results.
Reference links
Hirata disease
An autoimmune disease of endocrine system characterized by hypoglycemia caused by antibodies to insulin. This page summarizes how Hirata disease is classified and the care available at Weyland-Yutani Health System.
Also known as
- insulin autoimmune syndrome
Classification
Ontology identifier: DOID:0040100 (Human Disease Ontology).
Classification path: disease of anatomical entity › endocrine system disease › autoimmune disease of endocrine system.
Specialty: Immunology and Allergy
Broader conditions
Medical codes
Care at Weyland-Yutani Health System
Treatment of Hirata 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
Questions about Hirata disease? Call your nearest Weyland-Yutani location and ask for Immunology and Allergy.
Reference links