PedAM

Pediatric Disease Annotations & Medicines


	kimura disease

Disease ID	791
Disease	kimura disease
Definition	A chronic, benign, inflammatory condition that is characterized by the swelling of lymph node in the head and neck.
Synonym	disease, kimura eosinophilic granuloma of soft tissue eosinophilic hyperplastic lymphogranuloma eosinophilic hyperplastic lymphogranulomas eosinophilic lymphofollicular granuloma eosinophilic lymphofollicular granulomas eosinophilic lymphofolliculoses eosinophilic lymphofolliculosis granuloma, eosinophilic lymphofollicular granulomas, eosinophilic lymphofollicular hyperplastic lymphogranuloma, eosinophilic hyperplastic lymphogranulomas, eosinophilic kimura dis kimura's disease kimura's disease (disorder) lymphofollicular granuloma, eosinophilic lymphofollicular granulomas, eosinophilic lymphofolliculoses, eosinophilic lymphofolliculosis, eosinophilic lymphogranuloma, eosinophilic hyperplastic lymphogranulomas, eosinophilic hyperplastic
Orphanet	ORPHANET:482
DOID	DOID:7365
UMLS	C0033838
SNOMED-CT	SNOMEDCT_US_2016_09_01:399894006
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:9) C0018916 \| hemangioma \| 1 C0029882 \| otitis media \| 1 C0030326 \| panniculitis \| 1 C0022658 \| renal disease \| 1 C0017661 \| iga nephropathy \| 1 C0205788 \| epithelioid hemangioma \| 1 C0002989 \| angiolymphoid hyperplasia \| 1 C0029883 \| secretory otitis media \| 1 C0027726 \| nephrotic syndrome \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	(Waiting for update.)
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:40) 10344 \| CCL26 \| DISEASES 6361 \| CCL17 \| DISEASES 973 \| CD79A \| DISEASES 969 \| CD69 \| DISEASES 3565 \| IL4 \| DISEASES 3567 \| IL5 \| DISEASES 9173 \| IL1RL1 \| DISEASES 9113 \| LATS1 \| DISEASES 5989 \| RFX1 \| DISEASES 5156 \| PDGFRA \| DISEASES 2208 \| FCER2 \| DISEASES 59067 \| IL21 \| DISEASES 85407 \| NKD1 \| DISEASES 22925 \| PLA2R1 \| DISEASES 3815 \| KIT \| DISEASES 8209 \| C21orf33 \| DISEASES 6352 \| CCL5 \| DISEASES 1437 \| CSF2 \| DISEASES 6356 \| CCL11 \| DISEASES 6037 \| RNASE3 \| DISEASES 947 \| CD34 \| DISEASES 5553 \| PRG2 \| DISEASES 5319 \| PLA2G1B \| DISEASES 4327 \| MMP19 \| DISEASES 3039 \| HBA1 \| DISEASES 50616 \| IL22 \| DISEASES 5271 \| SERPINB8 \| DISEASES 5269 \| SERPINB6 \| DISEASES 85480 \| TSLP \| DISEASES 800 \| CALD1 \| DISEASES 1380 \| CR2 \| DISEASES 959 \| CD40LG \| DISEASES 5272 \| SERPINB9 \| DISEASES 90865 \| IL33 \| DISEASES 64109 \| CRLF2 \| DISEASES 5268 \| SERPINB5 \| DISEASES 55576 \| STAB2 \| DISEASES 387836 \| CLEC2A \| DISEASES 1232 \| CCR3 \| DISEASES 3684 \| ITGAM \| DISEASES
Locus	(Waiting for update.)

Disease ID	791
Disease	kimura disease
Integrated Phenotype	HPO \| Name(Total Integrated Phenotypes:5) HP:0001880 \| Eosinophilia HP:0003212 \| Increased IgE level HP:0010286 \| Abnormality of the salivary glands HP:0002716 \| Lymphadenopathy HP:0002729 \| Follicular hyperplasia
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:7) HP:0000100 \| Nephrosis \| 1 HP:0012490 \| Inflammation of fat tissue \| 1 HP:0001880 \| Eosinophilia \| 1 HP:0000388 \| Otitis media \| 1 HP:0002664 \| Neoplasia \| 1 HP:0001028 \| Strawberry mark \| 1 HP:0002835 \| Aspiration \| 1

Disease ID	791
Disease	kimura disease
Manually Symptom	UMLS \| Name(Total Manually Symptoms:2) C0403396 \| steroid-sensitive nephrotic syndrome C0027726 \| nephrotic syndrome
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:1) C0027726 \| nephrotic syndrome \| 1

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:0)
(Waiting for update.)

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.)

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