Congenital Horner syndrome

Symptom Information:

Symptom ID: HPO:0006837
Synonyms:
Congenital Horner syndrome [OMIM:Congenital Horner syndrome]
Quality:
Cross references:
OMIM: "Congenital Horner syndrome" [OMIM:Congenital Horner syndrome]
Is a (Direct Parents):
HPO         Horner syndrome
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system morphology(HPO:0012639)
             Abnormality of the autonomic nervous system(HPO:0002270)
                Abnormal autonomic nervous system physiology(HPO:0012332)
                   Horner syndrome(HPO:0002277)
                      Congenital Horner syndrome(HPO:0006837)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye physiology(HPO:0012373)
             Ptosis(HPO:0000508)
                Horner syndrome(HPO:0002277)
                   Congenital Horner syndrome(HPO:0006837)
          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)
                         Miosis(HPO:0000616)
                            Horner syndrome(HPO:0002277)
                               Congenital Horner syndrome(HPO:0006837)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Abnormality of the iris(HPO:0000525)
                      Abnormality of the pupil(HPO:0000615)
                         Miosis(HPO:0000616)
                            Horner syndrome(HPO:0002277)
                               Congenital Horner syndrome(HPO:0006837)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Congenital Horner syndrome (Orphanet:91413)