Limited extraocular movements

Symptom Information:

Symptom ID: HPO:0007941
Synonyms:
Limited extraocular movement [HPO:0007941]
Limited extraocular movements [OMIM:Limited extraocular movements]
Limited extraocular movements (1 family) [OMIM:Limited extraocular movements (1 family)]
Quality:
Cross references:
OMIM: "Limited extraocular movements" [OMIM:Limited extraocular movements]
OMIM: "Limited extraocular movements (1 family)" [OMIM:Limited extraocular movements (1 family)]
Is a (Direct Parents):
HPO         Abnormality of the extraocular muscles
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the extraocular muscles(HPO:0008049)
                Limited extraocular movements(HPO:0007941)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
Bilateral frontal polymicrogyria (Orphanet:208444)
CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASEDEFICIENCY 1 (OMIM:604377)
Fatal infantile cytochrome C oxidase deficiency (Orphanet:1561)
Perrault Syndrome (Orphanet:2855)
Perrault Syndrome 1 (OMIM:233400)
Polymicrogyria due to TUBB2B mutation (Orphanet:300573)