NDN Results

NDN

necdin, MAGE family member
05/31/2017

NDNF

neuron derived neurotrophic factor

congenital stationary night blindness 1B

MONDO_0009758 Condition
CSNB1B
10/15/2018

red color blindness

MONDO_0010565 Condition
Protan defect
03/07/2019

congenital stationary night blindness 1C

MONDO_0013183 Condition
congenital stationary night blindness 1C autosomal recessive
06/01/2017

congenital stationary night blindness 1E

MONDO_0013807 Condition
CSNB1E
10/16/2018

early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome

MONDO_0014371 Condition
Epileptic Encephalopathy, Early Infantile, type 23
10/23/2018

congenital stationary night blindness 1A

MONDO_0010690 Condition
congenital stationary night blindness type 1A
01/22/2020

congenital stationary night blindness 1D

MONDO_0013450 Condition
CSNB1D
10/16/2018

night blindness-skeletal anomalies-dysmorphism syndrome

MONDO_0015326 Condition
Hunter-Thompson-Reed syndrome

night blindness

MONDO_0004588 Condition
06/25/2018

congenital stationary night blindness

MONDO_0016293 Condition
congenital essential nyctalopia

red-green color blindness

MONDO_0010564 Condition
Reduced red-green discrimination

ectodermal dysplasia-blindness syndrome

MONDO_0010001 Condition

congenital stationary night blindness 1G

MONDO_0014614 Condition
CSNB1G

colorblindness, partial

MONDO_0000014 Condition

progressive microcephaly-seizures-cortical blindness-developmental delay syndrome

MONDO_0014714 Condition
Seizures, Cortical Blindness, Microcephaly Syndrome

blue color blindness

MONDO_0008610 Condition
Tritanopia

congenital stationary night blindness 1H

MONDO_0014872 Condition
CSNB1H
Additional Condition Matches

CYBERLINDNERA JADINII RNA

RXNORM:1432976 Drug