WormBase Tree Display for DO_term: DOID:0110867
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| DOID:0110867 | Name | congenital stationary night blindness 1C | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A congenital stationary night blindness characterized by autosomal recessive that has_material_basis_in homozygous or compound heterozygous mutation in the TRPM1 gene on chromosome 15q13-q14. | ||||
| Synonym | Exact | CSNB1C | |||
| congenital stationary night blindness 1C autosomal recessive | |||||
| Parent | Is_a | DOID:0050534 | |||
| DOID:0050737 | |||||
| DB_info | Database | OMIM | disease | 613216 | |
| Attribute_of | Gene_by_orthology | WBGene00001651 | |||
| WBGene00001795 | |||||
| WBGene00001796 |
