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WormBase Tree Display for DO_term: DOID:0110864

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Name Class

DOID:0110864Namecongenital stationary night blindness 1F
StatusValid
DefinitionA congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in compound heterozygous mutation in the LRIT3 gene on chromosome 4q25.
SynonymExactCSNB1F
congenital stationary night blindness 1F autosomal recessive
ParentIs_aDOID:0050534
DOID:0050737
DB_infoDatabaseOMIMdisease615058