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PedAM

Pediatric Disease Annotations & Medicines



   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:0002108Spontaneous pneumothoraxMP:0009862abnormal aorta elastic tissue morphology;HP:0001369Arthritis
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.)