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Disease
Symptom
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 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)
Abnormal eye physiology(HPO:0012373)
Ptosis(HPO:0000508)
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)