| lymphomatoid granulomatosis | ||||
| Disease ID | 1141 |
|---|---|
| Disease | lymphomatoid granulomatosis |
| Definition | An angiocentric and angiodestructive lymphoproliferative disorder primarily involving the lungs. It is caused by an Epstein-Barr virus-induced transformation of the B-cells, in a T-cell rich environment. Clinically and pathologically it resembles EXTRANODAL NK-T-CELL LYMPHOMA. |
| Synonym | [m] angiocentric immunoproliferative lesion [m]angiocentric immunoproliferative lesion ail angiocentric immunoproliferative lesion angiocentric immunoproliferative lesion (morphologic abnormality) angiocentric immunoproliferative lesions granulomatoses, lymphomatoid granulomatosis, lymphomatoid lg - lymphomatoid granulomatosis lyg lymphmatoid granulomatosis lymphoid granulomatosis lymphomatoid granulomatoses lymphomatoid granulomatosis (disorder) lymphomatoid granulomatosis (disorder) [ambiguous] lymphomatoid granulomatosis (grades i and ii) lymphomatoid granulomatosis [disease/finding] |
| Orphanet | |
| UMLS | C0024307 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:9) C0003873 | rheumatoid arthritis | 2 C0024115 | lung disease | 1 C0042384 | vasculitis | 1 C0442874 | neuropathy | 1 C0018202 | granulomatous vasculitis | 1 C0006413 | burkitt lymphoma | 1 C0024299 | lymphoma | 1 C0032285 | pneumonitis | 1 C0398794 | griscelli syndrome | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 1141 |
|---|---|
| Disease | lymphomatoid granulomatosis |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:5) HP:0001370 | Rheumatoid arthritis | 2 HP:0001744 | Splenomegaly | 1 HP:0030080 | Burkitt lymphoma | 1 HP:0002665 | Lymphoma | 1 HP:0002633 | Vasculitis | 1 |
| Disease ID | 1141 |
|---|---|
| Disease | lymphomatoid granulomatosis |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:12) C1332892 | sarcoma of the central nervous system C0751004 | giant intracranial aneurysms C0748159 | pulmonary involvement C0494491 | mononeuropathy C0233205 | halo sign C0162323 | polyarthritis C0149781 | spontaneous pneumothorax C0037299 | skin ulceration C0037285 | skin manifestation C0024299 | malignant lymphoma C0003864 | arthritis C0001175 | acquired immune deficiency syndrome |
| Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
|---|
| (Waiting for update.) |
All Snps(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
GWASdb Annotation(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
GWASdb Snp Trait(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
Mapped by lexical matching(Total Items:0) |
|---|
| (Waiting for update.) |
Mapped by homologous gene(Total Items:1) | ||||
|---|---|---|---|---|
| HP ID | HP Name | MP ID | MP Name | Annotation |
| HP:0002108 | Spontaneous pneumothorax | MP:0009862 | abnormal aorta elastic tissue morphology;HP:0001369 | Arthritis |
Chemical(Total Drugs:0) | |
|---|---|
| (Waiting for update.) | |
FDA approved drug and dosage information(Total Drugs:0) | |
|---|---|
| (Waiting for update.) | |
FDA labeling changes(Total Drugs:0) | |
|---|---|
| (Waiting for update.) | |