Optic nerve compression
Symptom Information:
Symptom ID: | HPO:0007807 | ||||
Synonyms: |
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Is a (Direct Parents): |
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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) 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) 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) MedDRA: |
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Database Frequency: | 6 / 7739 | ||||
Resource: |
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) |