You are using an outdated browser. Please upgrade your browser to improve your experience.

congenital nystagmus

Disease Summary
Associated Targets (4)
Tbio

3

Tchem

1


Explore Associated Targets
Mondo Description Nystagmus present at birth or caused by lesions sustained in utero or at the time of birth. It is usually pendular, and is associated with albinism and conditions characterized by early loss of central vision. Inheritance patterns may be X-linked, autosomal dominant, or recessive. (Adams et al., Principles of Neurology, 6th ed, p275)
Disease Ontology Description A pathologic nystagmus, present at birth, characterized by involuntary, rhythmic eye movements; oscillations are usually horizontal in direction.
Mondo Term and Equivalent IDs
MONDO:0005712:  congenital nystagmus
COHD:373489: 
DC:0000328: 
EFO:0007217: 
ICD10:H55.01: 
ICD9:379.51: 
MESH:D020417: 
OMIMPS:310700: 
SCTID:64635004: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Target Novelty (Tin-x)