PedAM

Pediatric Disease Annotations & Medicines


	autoimmune enteropathy

Disease ID	1684
Disease	autoimmune enteropathy
Definition	A rare disease in which certain cells in the intestine are destroyed by a patient's immune system. It causes severe, chronic, diarrhea and usually occurs in children.
Synonym	autoimmune enteropathy (disorder)
UMLS	C0341305
SNOMED-CT	SNOMEDCT_US_2016_09_01:235728001
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:6) C0011991 \| diarrhea \| 2 C0017178 \| gastrointestinal disorder \| 1 C0040053 \| thrombosis \| 1 C0040100 \| thymoma \| 1 C0021390 \| inflammatory bowel disease \| 1 C0011991 \| diarrhoea \| 1
Curated Gene	(Waiting for update.)
Inferring Gene	(Waiting for update.)
Text Mined Gene	(Waiting for update.)
Locus	(Waiting for update.)

Disease ID	1684
Disease	autoimmune enteropathy
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:7) HP:0002014 \| Diarrhea \| 2 HP:0100522 \| Thymoma \| 1 HP:0011473 \| Villous atrophy \| 1 HP:0002901 \| Hypocalcemia \| 1 HP:0002028 \| Chronic diarrhea \| 1 HP:0004936 \| Blood clot in vein \| 1 HP:0005305 \| Cerebral vein thrombosis \| 1

Disease ID	1684
Disease	autoimmune enteropathy
Manually Symptom	UMLS \| Name(Total Manually Symptoms:1) C0151945 \| cerebral venous thrombosis
Text Mined Symptom	UMLS \| Name \| Sentences' Count(Total Symptoms:1) C0151945 \| cerebral venous thrombosis \| 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.)

Web
Analytics