Horner syndrome

Symptom Information:

Symptom ID: HPO:0002277
Synonyms:
Horner's syndrome [HPO:0002277]
Horner syndrome [OMIM:Horner syndrome]
Horner's syndrome [OMIM:Horner's syndrome]
Horner's syndrome [MedDRA:10020392]
Quality:
Cross references:
OMIM: "Horner syndrome" [OMIM:Horner syndrome]
OMIM: "Horner's syndrome" [OMIM:Horner's syndrome]
Is a (Direct Parents):
HPO         Miosis
HPO         Abnormal autonomic nervous system physiology
MedDRA Structural change, deposit and degeneration of eye NEC
HPO         Ptosis
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye physiology(HPO:0012373)
             Ptosis(HPO:0000508)
                Horner syndrome(HPO:0002277)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                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)
                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)
       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)
MedDRA:
Eye disorders(MedDRA:10015919)
    Ocular structural change, deposit and degeneration NEC(MedDRA:10042261)
       Structural change, deposit and degeneration of eye NEC(MedDRA:10042260)
          Horner syndrome(HPO:0002277)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Hereditary neurocutaneous angioma (Orphanet:1062)
NEUROBLASTOMA, SUSCEPTIBILITY TONEUROBLASTOMA, SUSCEPTIBILITY TO, 1, INCLUDED (OMIM:256700)
Neuroblastoma (Orphanet:635)
PHACE syndrome (Orphanet:42775)
Primary basilar impression (Orphanet:2285)
Progressive hemifacial atrophy (Orphanet:1214)
Syringomyelia (Orphanet:3280)