PedAM
Pediatric Disease Annotations & Medicines
| pulmonary hemosiderosis | ||||
| Disease ID | 1449 |
|---|---|
| Disease | pulmonary hemosiderosis |
| Synonym | brown induration of lung essential brown induration of lung hemosiderosis pulmonary hemosiderosis, pulmonary, idiopathic hemosiderosis, pulmonary, with deficiency of gamma-a globulin idio pulm hemosiderosis idiopathic pulmonary haemosiderosis idiopathic pulmonary haemosiderosis (disorder) idiopathic pulmonary hemosiderosis idiopathic pulmonary hemosiderosis (disorder) iph - idiopathic pulmonary haemosiderosis iph - idiopathic pulmonary hemosiderosis lung, essential brown induration pulmonary haemosiderosis |
| Orphanet | |
| OMIM | |
| DOID | |
| ICD10 | |
| UMLS | C0020807 |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:11) C0007570 | celiac disease | 5 C0162316 | iron-deficiency anemia | 1 C0004096 | asthma | 1 C0024115 | lung disease | 1 C0155877 | allergic asthma | 1 C0553662 | juvenile idiopathic arthritis | 1 C0035229 | respiratory insufficiency | 1 C0006287 | bronchopulmonary dysplasia | 1 C0003864 | arthritis | 1 C0035439 | rheumatic heart disease | 1 C0002871 | anemia | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:15) 4282 | MIF | DISEASES 973 | CD79A | DISEASES 4353 | MPO | DISEASES 5657 | PRTN3 | DISEASES 4069 | LYZ | DISEASES 8626 | TP63 | DISEASES 10938 | EHD1 | DISEASES 3855 | KRT7 | DISEASES 23762 | OSBP2 | DISEASES 4582 | MUC1 | DISEASES 959 | CD40LG | DISEASES 6005 | RHAG | DISEASES 2155 | F7 | DISEASES 54790 | TET2 | DISEASES 727897 | MUC5B | DISEASES |
| Locus | (Waiting for update.) |
| Disease ID | 1449 |
|---|---|
| Disease | pulmonary hemosiderosis |
| Integrated Phenotype | HPO | Name(Total Integrated Phenotypes:8) HP:0006535 | Recurrent intrapulmonary hemorrhage HP:0002206 | Pulmonary fibrosis HP:0002093 | progressive respiratory failure HP:0002720 | Decreased immunoglobulin A HP:0002105 | Hemoptysis HP:0002086 | Respiratory abnormality HP:0001891 | Iron-deficiency anemia HP:0005828 | Transient pulmonary infiltrates |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:7) HP:0002608 | Celiac disease | 5 HP:0001891 | Iron-deficiency anemia | 1 HP:0005681 | Juvenile idiopathic arthritis | 1 HP:0001369 | Arthritis | 1 HP:0002099 | Asthma | 1 HP:0001903 | Anemia | 1 HP:0002093 | progressive respiratory failure | 1 |
| Disease ID | 1449 |
|---|---|
| Disease | pulmonary hemosiderosis |
| Manually Symptom | (Waiting for update.) |
| Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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| (Waiting for update.) |
All Snps(Total Genotypes:0) | |
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| (Waiting for update.) | |
GWASdb Annotation(Total Genotypes:0) | |
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| (Waiting for update.) | |
GWASdb Snp Trait(Total Genotypes:0) | |
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| (Waiting for update.) | |
Mapped by lexical matching(Total Items:0) |
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| (Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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| (Waiting for update.) |
Chemical(Total Drugs:0) | |
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| (Waiting for update.) | |
FDA approved drug and dosage information(Total Drugs:0) | |
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FDA labeling changes(Total Drugs:0) | |
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| (Waiting for update.) | |