WormBase Tree Display for DO_term: DOID:0110864
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DOID:0110864 | Name | congenital stationary night blindness 1F | |||
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Status | Valid | ||||
Definition | A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in compound heterozygous mutation in the LRIT3 gene on chromosome 4q25. | ||||
Synonym | Exact | CSNB1F | |||
congenital stationary night blindness 1F autosomal recessive | |||||
Parent | Is_a | DOID:0050534 | |||
DOID:0050737 | |||||
DB_info | Database | OMIM | disease | 615058 |