congenital stationary night blindness 1C (Q32144049)
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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
Language | Label | Description | Also known as |
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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 |
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