Optic nerve compression

Symptom Information:

Symptom ID: HPO:0007807
Optic nerve compression [OMIM:Optic nerve compression]
Cross references:
OMIM: "Optic nerve compression" [OMIM:Optic nerve compression]
Is a (Direct Parents):
HPO         Cranial nerve compression
HPO         Abnormality of the optic nerve
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the posterior segment of the globe(HPO:0004329)
                   Abnormality of the fundus(HPO:0001098)
                      Abnormality of the optic nerve(HPO:0000587)
                         Optic nerve compression(HPO:0007807)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system morphology(HPO:0012639)
             Morphological abnormality of the central nervous system(HPO:0002011)
                Abnormality of the cranial nerves(HPO:0001291)
                   Cranial nerve compression(HPO:0001293)
                      Optic nerve compression(HPO:0007807)
Database Frequency: 6 / 7739

All diseases associated with this symptom:

Camurati-Engelmann disease (Orphanet:1328)
Hurler-Scheie syndrome (Orphanet:93476)
Mucopolysaccharidosis type 2 (Orphanet:580)
Osteopetrosis - hypogammaglobulinemia (Orphanet:178389)
Osteopetrosis with renal tubular acidosis (Orphanet:2785)
Scheie syndrome (Orphanet:93474)