WormBase Tree Display for DO_term: DOID:0110867
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DOID:0110867 | Name | congenital stationary night blindness 1C | |||
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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 (2) | ||||
Parent | Is_a | DOID:0050534 | |||
DOID:0050737 | |||||
DB_info | Database | OMIM | disease | 613216 | |
Attribute_of | Gene_by_orthology | WBGene00001651 | |||
WBGene00001795 | |||||
WBGene00001796 |