Pendular nystagmus

Symptom Information:

Symptom ID: HPO:0012043
Synonyms:
NYSTAGMUS, CONTINUOUS PENDULAR [HPO:0012043]
NYSTAGMUS, PENDULAR [HPO:0012043]
Nystagmus, continuous pendular [OMIM:Nystagmus, continuous pendular]
Nystagmus, pendular [OMIM:Nystagmus, pendular]
Pendular nystagmus [OMIM:Pendular nystagmus]
Nystagmus, pendular (primarily in childhood) [OMIM:Nystagmus, pendular (primarily in childhood)]
Quality:
Cross references:
OMIM: "Nystagmus, continuous pendular" [OMIM:Nystagmus, continuous pendular]
OMIM: "Nystagmus, pendular" [OMIM:Nystagmus, pendular]
OMIM: "Pendular nystagmus" [OMIM:Pendular nystagmus]
OMIM: "Nystagmus, pendular (primarily in childhood)" [OMIM:Nystagmus, pendular (primarily in childhood)]
Is a (Direct Parents):
HPO         Nystagmus
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)
                      Pendular nystagmus(HPO:0012043)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
Blue cone monochromatism (Orphanet:16)
CHROMOSOME 2q31.1 DUPLICATION SYNDROME (OMIM:613681)
Congenital blindness due to retinal non-attachment (Orphanet:300337)
Leber congenital amaurosis 4 (OMIM:604393)
Leber congenital amaurosis 6 (OMIM:613826)
Leber congenital amaurosis 7 (OMIM:613829)
Leber congenital amaurosis 8 (OMIM:613835)
MICROPHTHALMIA, SYNDROMIC 13 (OMIM:300915)
NYSTAGMUS 1, CONGENITAL, X-LINKED (OMIM:310700)
STRIATONIGRAL DEGENERATION, INFANTILE (OMIM:271930)