Optic atrophy from cranial nerve compression

Symptom Information:

Symptom ID: HPO:0007958
Synonyms:
Optic atrophy from cranial nerve compression [OMIM:Optic atrophy from cranial nerve compression]
Quality:
Cross references:
OMIM: "Optic atrophy from cranial nerve compression" [OMIM:Optic atrophy from cranial nerve compression]
Is a (Direct Parents):
HPO         Optic atrophy
HPO         Cranial nerve compression
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 posterior segment of the globe(HPO:0004329)
                   Abnormality of the fundus(HPO:0001098)
                      Abnormality of the optic nerve(HPO:0000587)
                         Optic atrophy(HPO:0000648)
                            Optic atrophy from cranial nerve compression(HPO:0007958)
       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 atrophy from cranial nerve compression(HPO:0007958)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

HYPEROSTOSIS CORTICALIS GENERALISATA (OMIM:239100)
Hyperostosis corticalis generalisata (Orphanet:3416)