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PedAM

Pediatric Disease Annotations & Medicines



   pulmonary arteriovenous fistulas
  

Disease ID 795
Disease pulmonary arteriovenous fistulas
Definition
A congenital or acquired malformation characterized by abnormal communication between the pulmonary arteries and pulmonary veins in the lungs.
Synonym
arterioven fistu pul ves
arteriovenous fistula of pulmonary vessels
arteriovenous fistula of pulmonary vessels (disorder)
arteriovenous fistulas pulmonary
fistula, arteriovenous, pulmonary
pulmonary arterio-venous fistula
pulmonary arteriovenous fistula
pulmonary arteriovenous malformation
pulmonary av fistula
Orphanet
OMIM
ICD10
UMLS
C0155675
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:13)
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 795
Disease pulmonary arteriovenous fistulas
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:4)
HP:0100759  |  Finger clubbing
HP:0004952  |  Pulmonary arteriovenous fistulas
HP:0100760  |  Clubbing of toes
HP:0000961  |  Cyanosis
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:18)
HP:0001009  |  Telangiectases  |  6
HP:0012418  |  Low blood oxygen level  |  5
HP:0000961  |  Cyanosis  |  3
HP:0001694  |  Right-to-left shunt  |  2
HP:0012151  |  Hemothorax  |  2
HP:0001297  |  Cerebral vascular events  |  2
HP:0002617  |  Aneurysmal dilatation  |  1
HP:0001649  |  Tachycardia  |  1
HP:0030049  |  Brain abscess  |  1
HP:0012173  |  Postural tachycardia  |  1
HP:0001750  |  Single ventricle  |  1
HP:0002076  |  Migraine headaches  |  1
HP:0002664  |  Neoplasia  |  1
HP:0002326  |  TIA  |  1
HP:0030853  |  Heterotaxy  |  1
HP:0001719  |  Double-outlet right ventricle  |  1
HP:0010316  |  Ebstein's anomaly of the tricuspid valve  |  1
HP:0012735  |  Coughing  |  1
Disease ID 795
Disease pulmonary arteriovenous fistulas
Manually Symptom
UMLS  | Name(Total Manually Symptoms:2)
C0010520  |  cyanosis
C0006105  |  brain abscess
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:1)
C0010520  |  cyanosis  |  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.)