Miosis
Symptom Information:
Symptom ID: | HPO:0000616 | |||||||||||||||||
Synonyms: |
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Cross references: |
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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 eye(HPO:0000478) 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) Abnormality of the uvea(HPO:0000553) Abnormality of the iris(HPO:0000525) Abnormality of the pupil(HPO:0000615) Miosis(HPO:0000616) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Pupillary signs(MedDRA:10037533) Miosis(HPO:0000616) |
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Database Frequency: | 11 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
Aromatic L-amino acid decarboxylase deficiency | (Orphanet:35708) |
CLUSTER HEADACHE, FAMILIAL | (OMIM:119915) |
Congenital microcoria | (Orphanet:566) |
MICROPHTHALMIA, ISOLATED, WITH CATARACT 1 | (OMIM:156850) |
MYOPATHY, TUBULAR AGGREGATE, 2 | (OMIM:615883) |
Microphthalmia - cataract | (Orphanet:2543) |
OPHTHALMOPLEGIA TOTALIS WITH PTOSIS AND MIOSIS | (OMIM:258400) |
OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY | (OMIM:212550) |
Refsum disease | (Orphanet:773) |
Spastic ataxia with congenital miosis | (Orphanet:1182) |
Stormorken-Sjaastad-Langslet syndrome | (Orphanet:3204) |