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congenital nystagmus
Disease Summary
Associated Targets (4)
Tbio
3
Tclin
1
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.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
COHD:373489
DC:0000328
DOID:9649
EFO:0007217
ICD10:H55.01
ICD9:379.51
MESH:D020417
OMIMPS:310700
SCTID:64635004
MONDO:0005712
High level summary of knowledge for a disease, including descriptions and datasource references.