eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| riboflavin deficiency | ||||
| Disease ID | 1089 |
|---|---|
| Disease | riboflavin deficiency |
| Definition | A dietary deficiency of riboflavin causing a syndrome chiefly marked by cheilitis, angular stomatitis, glossitis associated with a purplish red or magenta-colored tongue that may show fissures, corneal vascularization, dyssebacia, and anemia. (Dorland, 27th ed) |
| Synonym | ariboflavinosis ariboflavinosis (disorder) b2 deficiencies vitamin b2 deficiency vitamin defic riboflavin deficiencies, riboflavin deficiency riboflavin deficiency, riboflavin rbfvd riboflavin defic riboflavin deficiencies riboflavin deficiency [disease/finding] riboflavine deficiency vitamin b2 deficiency |
| OMIM | |
| DOID | |
| ICD10 | |
| UMLS | C0035528 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:2) |
| Curated Gene | Entrez_id | Symbol | Resource(Total Genes:1) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:10) 1528 | CYB5A | 3.3 | DISEASES 2042 | EPHA3 | 3.28 | DISEASES 2149 | F2R | 2.796 | DISEASES 3146 | HMGB1 | 2.048 | DISEASES 3303 | HSPA1A | 2.444 | DISEASES 4524 | MTHFR | 1.356 | DISEASES 5950 | RBP4 | 2.43 | DISEASES 7018 | TF | 1.126 | DISEASES 7099 | TLR4 | 1.279 | DISEASES 10333 | TLR6 | 3.094 | DISEASES |
| Locus | (Waiting for update.) |
| Disease ID | 1089 |
|---|---|
| Disease | riboflavin deficiency |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:1) |
| Disease ID | 1089 |
|---|---|
| Disease | riboflavin deficiency |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:1) C0221264 | cheilosis |
| Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
|---|
| (Waiting for update.) |
Text Mining Genotype(Total 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.) |
| Disease ID | 1089 |
|---|---|
| Disease | riboflavin deficiency |
| Case | (Waiting for update.) |