Anisocoria

Symptom Information:

Symptom ID: HPO:0009916
Synonyms:
Asymmetric pupil sizes [HPO:0009916]
Asymmetry of the pupils [HPO:0009916]
Anisocoria [OMIM:Anisocoria]
Asymmetric pupil sizes [OMIM:Asymmetric pupil sizes]
Anisocoria (in 1 patient) [OMIM:Anisocoria (in 1 patient)]
Anisocoria (in some patients) [OMIM:Anisocoria (in some patients)]
Anisocoria (unequal pupal size) [OMIM:Anisocoria (unequal pupal size)]
Quality:
Cross references:
OMIM: "Anisocoria" [OMIM:Anisocoria]
OMIM: "Asymmetric pupil sizes" [OMIM:Asymmetric pupil sizes]
OMIM: "Anisocoria (in 1 patient)" [OMIM:Anisocoria (in 1 patient)]
OMIM: "Anisocoria (in some patients)" [OMIM:Anisocoria (in some patients)]
OMIM: "Anisocoria (unequal pupal size)" [OMIM:Anisocoria (unequal pupal size)]
UMLS:C0003079 "Anisocoria" [HPO:0009916]
Is a (Direct Parents):
HPO         Abnormality of the pupil
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 globe(HPO:0012374)
                Abnormality of the uvea(HPO:0000553)
                   Abnormality of the iris(HPO:0000525)
                      Abnormality of the pupil(HPO:0000615)
                         Anisocoria(HPO:0009916)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Abnormality of the iris(HPO:0000525)
                      Abnormality of the pupil(HPO:0000615)
                         Anisocoria(HPO:0009916)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME (OMIM:231550)
ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME (OMIM:615510)
ANISOCORIA (OMIM:106240)
Citrullinemia type II (Orphanet:247585)
EXFOLIATION SYNDROME (OMIM:177650)
FACIAL SPASM (OMIM:134300)
Intellectual deficit - alacrima - achalasia (Orphanet:289483)
OPHTHALMOPLEGIA, FAMILIAL STATIC (OMIM:165000)
Senior-Boichis syndrome (Orphanet:84081)
Triple A syndrome (Orphanet:869)