Miosis

Symptom Information:

Symptom ID: HPO:0000616
Synonyms:
Myosis [Orphanet:4120]
Constricted pupil (finding) [Orphanet:4120]
Pupil constriction (observable entity) [Orphanet:4120]
Miosis disorder [Orphanet:4120]
Pupil constriction observed [Orphanet:4120]
Miosis [OMIM:Miosis]
Pupillary anomalies/mydriasis/myosis/tonic pupil [Orphanet:4120]
Pupils constricted [Orphanet:4120]
Constricted pupils [Orphanet:4120]
Miosis [Orphanet:4120]
Miosis [MedDRA:10027646]
Constricted pupils [MedDRA:10027646]
Miosis (persistent), not due to miotics [MedDRA:10027646]
Pin-point pupils [MedDRA:10027646]
Pupils constricted [MedDRA:10027646]
Pupils pinpoint [MedDRA:10027646]
Tonic pupillary reaction [MedDRA:10027646]
Quality:
Cross references:
Orphanet:4120 "Pupillary anomalies/mydriasis/myosis/tonic pupil" [Orphanet:4120]
OMIM: "Miosis" [OMIM:Miosis]
UMLS:C0728710 "Miosis" [HPO:0000616]
UMLS:C0026205 "Miosis disorder" [Orphanet:4120]
UMLS:C0728710 "Pupil constriction observed" [Orphanet:4120]
Is a (Direct Parents):
Orphanet Abnormality of the pupil
MedDRA Pupillary signs
HPO         Abnormality of the pupil
Orphanet Abnormality of the eye
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)
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)