Rank (Similarity) |
PMID (PMCID) |
---|
|
Total: 9
HPO ID | Term | Frequency |
---|---|---|
HP:0000505 | Visual impairment | Frequent (79-30%) |
HP:0001131 | Corneal dystrophy | Frequent (79-30%) |
HP:0001251 | Ataxia | Frequent (79-30%) |
HP:0002073 | Progressive cerebellar ataxia | Frequent (79-30%) |
HP:0002342 | Intellectual disability, moderate | Frequent (79-30%) |
HP:0002493 | Upper motor neuron dysfunction | Frequent (79-30%) |
HP:0002503 | Spinocerebellar tract degeneration | Frequent (79-30%) |
HP:0007006 | Dorsal column degeneration | Frequent (79-30%) |
HP:0007957 | Corneal opacity | Frequent (79-30%) |
Total: 0
HPO ID | Term | # of case reports |
---|
Total: 0
Gene Symbol | Gene Name | Entrez Gene ID |
---|