(Q32144049)
English
congenital stationary night blindness 1C
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
- CSNB1C
- congenital stationary night blindness 1C autosomal recessive
- NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C
- congenital stationary night blindness type 1C
- NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C; CSNB1C
- Csnb, Complete, Autosomal Recessive
Statements
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Identifiers
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