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Browse result for autosomal recessive congenital nystagmus
※ introduction A congenital nystagmus characterized by autosomal recessive inheritance.
Reference
DiseaseOntology: autosomal recessive congenital nystagmus
Reference
DiseaseOntology: autosomal recessive congenital nystagmus
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD00113 | Q9Y6N7 | 6091 | ROBO1 | Roundabout homolog 1 | Homo sapiens |
| PTMD08599 | Q6ZUT3 | 90167 | FRMD7 | FERM domain-containing protein 7 | Homo sapiens |