| troyer syndrome | ||||
| Disease ID | 1880 |
|---|---|
| Disease | troyer syndrome |
| Synonym | cross-mckusick syndrome spastic paraparesis, childhood onset, with distal muscle wasting spastic paraparesis, childhood-onset, with distal muscle wasting spastic paraplegia 20, autosomal recessive spastic paraplegia with distal muscle wasting spastic paraplegia, autosomal recessive, troyer type spg20 troyer syndrome (disorder) |
| OMIM | |
| DOID | |
| UMLS | C0393559 |
| SNOMED-CT | |
| Curated Gene | Entrez_id | Symbol | Resource(Total Genes:1) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:22) 10226 | PLIN3 | DISEASES 5444 | PON1 | DISEASES 1327 | COX4I1 | DISEASES 27338 | UBE2S | DISEASES 11059 | WWP1 | DISEASES 123 | PLIN2 | DISEASES 4131 | MAP1B | DISEASES 3313 | HSPA9 | DISEASES 5346 | PLIN1 | DISEASES 27173 | SLC39A1 | DISEASES 4691 | NCL | DISEASES 6683 | SPAST | DISEASES 3309 | HSPA5 | DISEASES 9798 | IST1 | DISEASES 23111 | SPG20 | DISEASES 1822 | ATN1 | DISEASES 91252 | SLC39A13 | DISEASES 2060 | EPS15 | DISEASES 83737 | ITCH | DISEASES 84701 | COX4I2 | DISEASES 7337 | UBE3A | DISEASES 10908 | PNPLA6 | DISEASES |
| Locus | (Waiting for update.) |
| Disease ID | 1880 |
|---|---|
| Disease | troyer syndrome |
| Integrated Phenotype | (Waiting for update.) |
| Text Mined Phenotype | (Waiting for update.) |
| Disease ID | 1880 |
|---|---|
| Disease | troyer syndrome |
| 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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GWASdb Annotation(Total Genotypes:0) | |
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GWASdb Snp Trait(Total Genotypes:0) | |
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| (Waiting for update.) | |
Mapped by lexical matching(Total Items:0) |
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Mapped by homologous gene(Total Items:0) |
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Chemical(Total Drugs:0) | |
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FDA approved drug and dosage information(Total Drugs:0) | |
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FDA labeling changes(Total Drugs:0) | |
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