Lens subluxation
Symptom Information:
Symptom ID: | HPO:0001132 | ||||||||||||||||||||||||||||
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 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 lens(HPO:0000517) Ectopia lentis(HPO:0001083) Lens subluxation(HPO:0001132) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Eye disorders congenital(MedDRA:10015920) Lens disorders congenital(MedDRA:10024205) Lens subluxation(HPO:0001132) Injury, poisoning and procedural complications(MedDRA:10022117) Injuries NEC(MedDRA:10022114) Eye injuries NEC(MedDRA:10027674) Lens subluxation(HPO:0001132) |
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Database Frequency: | 13 / 7739 | ||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
COLOBOMA, OCULAR, AUTOSOMAL RECESSIVE | (OMIM:216820) |
EXFOLIATION SYNDROME | (OMIM:177650) |
Focal dermal hypoplasia | (Orphanet:2092) |
Glaucoma - ectopia - microspherophakia - stiff joints - short stature | (Orphanet:2084) |
Hyperlysinemia, type I | (OMIM:238700) |
KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS | (OMIM:245160) |
Late-onset localized junctional epidermolysis bullosa - intellectual deficit | (Orphanet:231556) |
MARFANOID HABITUS WITH SITUS INVERSUS | (OMIM:609008) |
MEGALOCORNEA | (OMIM:309300) |
MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION | (OMIM:614292) |
Microspherophakia - metaphyseal dysplasia | (Orphanet:2551) |
Temtamy syndrome | (Orphanet:1777) |
WEILL-MARCHESANI SYNDROME 1 | (OMIM:277600) |