Congenital nystagmus

Symptom Information:

Symptom ID: HPO:0006934
Synonyms:
NYSTAGMUS, CONGENITAL [HPO:0006934]
Congenital nystagmus [OMIM:Congenital nystagmus]
Nystagmus, congenital [OMIM:Nystagmus, congenital]
Congenital nystagmus [MedDRA:10010562]
Quality:
Cross references:
OMIM: "Congenital nystagmus" [OMIM:Congenital nystagmus]
OMIM: "Nystagmus, congenital" [OMIM:Nystagmus, congenital]
Is a (Direct Parents):
HPO         Nystagmus
MedDRA Coordination and balance disturbances
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye physiology(HPO:0012373)
             Abnormality of eye movement(HPO:0000496)
                Abnormal involuntary eye movements(HPO:0012547)
                   Nystagmus(HPO:0000639)
                      Congenital nystagmus(HPO:0006934)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Neurological disorders NEC(MedDRA:10029305)
       Coordination and balance disturbances(MedDRA:10072984)
          Congenital nystagmus(HPO:0006934)
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Aplasia cutis - myopia (Orphanet:1117)
Autosomal recessive spastic paraplegia type 48 (Orphanet:306511)
Diabetic embryopathy (Orphanet:1926)
Foveal hypoplasia - presenile cataract (Orphanet:2253)
Hermansky-Pudlak syndrome type 9 (Orphanet:280663)
Karsch-Neugebauer syndrome (Orphanet:2329)
Leber congenital amaurosis 15 (OMIM:613843)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
NYSTAGMUS 1, CONGENITAL, X-LINKED (OMIM:310700)
NYSTAGMUS, CONGENITAL, AUTOSOMAL RECESSIVE (OMIM:257400)