Online Mendelian Inheritance in Man

Last uploaded: August 28, 2024
Preferred Name

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A
Synonyms

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2

CSNB2

CSNB, INCOMPLETE, X-LINKED

CSNB2A

ID

http://purl.bioontology.org/ontology/OMIM/300071

altLabel

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2

CSNB2

CSNB, INCOMPLETE, X-LINKED

CSNB2A

cui

C1848172

Gene Locus

Xp11.23

Gene Symbol

CORDX3

CSNB2

AIED

CSNB2A

CACNA1F

OA2

MIMTYPEMEANING

Phenotype description, molecular basis known.

Moved from

600603

notation

300071

OMIM Entry Type

3

OMIM MimType Value

pound

prefLabel

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A

tui

T047

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