congenital stationary night blindness 1F (Q32144004)

From Wikidata
Jump to navigation Jump to search
congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in compound heterozygous mutation in the LRIT3 gene on chromosome 4q25
  • CSNB1F
  • congenital stationary night blindness 1F autosomal recessive
  • NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F
  • congenital stationary night blindness type 1F
  • NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F; CSNB1F
edit
Language Label Description Also known as
English
congenital stationary night blindness 1F
congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in compound heterozygous mutation in the LRIT3 gene on chromosome 4q25
  • CSNB1F
  • congenital stationary night blindness 1F autosomal recessive
  • NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F
  • congenital stationary night blindness type 1F
  • NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F; CSNB1F

Statements

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit