eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| beryllium disease | ||||
| Disease ID | 1765 |
|---|---|
| Disease | beryllium disease |
| Definition | A form of pneumoconiosis caused by inhaled rare metal BERYLLIUM or its soluble salts which are used in a wide variety of industry including alloys, ceramics, radiographic equipment, and vacuum tubes. Berylliosis is characterized by an acute inflammatory reaction in the upper airway leading to BRONCHIOLITIS; PULMONARY EDEMA; and pneumonia. |
| Synonym | beryllioses berylliosis berylliosis (disorder) berylliosis [disease/finding] beryllium poisoning |
| Orphanet | |
| DOID | |
| ICD10 | |
| UMLS | C0005138 |
| MeSH | |
| SNOMED-CT | |
| Curated Gene | Entrez_id | Symbol | Resource(Total Genes:11) |
| Inferring Gene | Entrez_id | Symbol | Resource(Total Genes:15) 56244 | BTNL2 | CIPHER;CTD_human 2729 | GCLC | CIPHER 2730 | GCLM | CIPHER;CTD_human 3113 | HLA-DPA1 | CIPHER 3115 | HLA-DPB1 | CIPHER;CTD_human 3117 | HLA-DQA1 | CIPHER 3119 | HLA-DQB1 | CIPHER 3123 | HLA-DRB1 | CIPHER;CTD_human 7040 | TGFB1 | CIPHER;CTD_human 7124 | TNF | CIPHER;CTD_human 3116 | HLA-DPB2 | CTD_human 3569 | IL6 | CTD_human 940 | CD28 | CTD_human 3559 | IL2RA | CTD_human 1636 | ACE | CTD_human |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:15) 5476 | CTSA | 2.119 | DISEASES 728441 | GGT2 | 1.192 | DISEASES 2876 | GPX1 | 1.822 | DISEASES 2877 | GPX2 | 2.664 | DISEASES 2878 | GPX3 | 2.242 | DISEASES 9446 | GSTO1 | 2.354 | DISEASES 2950 | GSTP1 | 1.168 | DISEASES 9146 | HGS | 2.843 | DISEASES 3108 | HLA-DMA | 2.762 | DISEASES 3113 | HLA-DPA1 | 3.119 | DISEASES 3115 | HLA-DPB1 | 4.338 | DISEASES 3123 | HLA-DRB1 | 1.24 | DISEASES 51270 | TFDP3 | 2.949 | DISEASES 7124 | TNF | 1.631 | DISEASES 8718 | TNFRSF25 | 1.074 | DISEASES |
| Locus | (Waiting for update.) |
| Disease ID | 1765 |
|---|---|
| Disease | beryllium disease |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | (Waiting for update.) |
| Disease ID | 1765 |
|---|---|
| Disease | beryllium disease |
| 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.) |
Text Mining Genotype(Total 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) | |
|---|---|
| (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.) |
| Disease ID | 1765 |
|---|---|
| Disease | beryllium disease |
| Case | (Waiting for update.) |