eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| lacrimoauriculodentodigital syndrome | ||||
| Disease ID | 1613 |
|---|---|
| Disease | lacrimoauriculodentodigital syndrome |
| Synonym | lacrimo-auriculo-dento-digital syndrome ladd ladd syndrome levy hollister syndrome levy-hollister syndrome levy-hollister syndrome (disorder) |
| Orphanet | |
| OMIM | |
| DOID | |
| UMLS | C0265269 |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:1) |
| Curated Gene | Entrez_id | Symbol | Resource(Total Genes:3) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:10) 57492 | ARID1B | 3.101 | DISEASES 2259 | FGF14 | 3.838 | DISEASES 2248 | FGF3 | 3.805 | DISEASES 2253 | FGF8 | 2.616 | DISEASES 2254 | FGF9 | 3.076 | DISEASES 2260 | FGFR1 | 1.578 | DISEASES 2263 | FGFR2 | 4.438 | DISEASES 2261 | FGFR3 | 3.331 | DISEASES 2591 | GALNT3 | 2.443 | DISEASES 29968 | PSAT1 | 1.561 | DISEASES |
| Locus | Symbol | Locus(Total Locus:3) |
| Disease ID | 1613 |
|---|---|
| Disease | lacrimoauriculodentodigital syndrome |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:3) |
| Disease ID | 1613 |
|---|---|
| Disease | lacrimoauriculodentodigital syndrome |
| Manually Symptom | (Waiting for update.) |
| 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 | 1613 |
|---|---|
| Disease | lacrimoauriculodentodigital syndrome |
| Case | (Waiting for update.) |