Ectopia lentis

Symptom Information:

Symptom ID: HPO:0001083
Synonyms:
Abnormality of lens position [HPO:0001083]
Dislocated lens [HPO:0001083]
Dislocated lenses [HPO:0001083]
Lens dislocation [HPO:0001083]
Lens dislocation [Orphanet:4720]
Subluxation of lens (disorder) [Orphanet:4720]
Congenital ectopic lens (disorder) [Orphanet:4720]
Ectopia Lentis [Orphanet:4720]
Lens Subluxation [Orphanet:4720]
Luxation of lens [Orphanet:4720]
Dislocated lens [OMIM:Dislocated lens]
Dislocated lenses [OMIM:Dislocated lenses]
Ectopia lentis [OMIM:Ectopia lentis]
Lens dislocation [OMIM:Lens dislocation]
Lens dislocation/luxation/subluxation/ectopia lentis [Orphanet:4720]
Lens luxation [Orphanet:4720]
Subluxation of lens [Orphanet:4720]
Ectopia lentis [Orphanet:4720]
Lens dislocation [MedDRA:10024203]
Anterior dislocation of lens [MedDRA:10024203]
Dislocated lens [MedDRA:10024203]
Posterior dislocation of lens [MedDRA:10024203]
Subluxation of lens [MedDRA:10024203]
Lens luxation [MedDRA:10024203]
Lens abnormality, congenital [MedDRA:10024202]
Congenital anomalies of lens shape [MedDRA:10024202]
Congenital ectopic lens [MedDRA:10024202]
Congenital lens anomaly NOS [MedDRA:10024202]
Ectopia lentis [MedDRA:10024202]
Dislocated lens (upward) [OMIM:Dislocated lens (upward)]
Ectopia lentis (6%) [OMIM:Ectopia lentis (6%)]
Ectopia lentis (64%) [OMIM:Ectopia lentis (64%)]
Ectopia lentis (84%) [OMIM:Ectopia lentis (84%)]
Ectopia lentis (in some patients) [OMIM:Ectopia lentis (in some patients)]
Lens subluxation (in some patients) [OMIM:Lens subluxation (in some patients)]
Quality:
Cross references:
HPO:0000665 "Abnormality of lens position" [Orphanet:4720]
HPO:0001132 "Lens subluxation" [Orphanet:4720]
Orphanet:4720 "Lens dislocation/luxation/subluxation/ectopia lentis" [Orphanet:4720]
OMIM: "Dislocated lens" [OMIM:Dislocated lens]
OMIM: "Dislocated lenses" [OMIM:Dislocated lenses]
OMIM: "Ectopia lentis" [OMIM:Ectopia lentis]
OMIM: "Lens dislocation" [OMIM:Lens dislocation]
OMIM: "Dislocated lens (upward)" [OMIM:Dislocated lens (upward)]
OMIM: "Ectopia lentis (6%)" [OMIM:Ectopia lentis (6%)]
OMIM: "Ectopia lentis (64%)" [OMIM:Ectopia lentis (64%)]
OMIM: "Ectopia lentis (84%)" [OMIM:Ectopia lentis (84%)]
OMIM: "Ectopia lentis (in some patients)" [OMIM:Ectopia lentis (in some patients)]
OMIM: "Lens subluxation (in some patients)" [OMIM:Lens subluxation (in some patients)]
UMLS:C0013581 "Ectopia Lentis" [Orphanet:4720]
UMLS:C0023316 "Lens Subluxation" [Orphanet:4720]
UMLS:C1827700 "Luxation of lens" [Orphanet:4720]
UMLS:C0023309 "Lens dislocation" [Orphanet:4720]
Is a (Direct Parents):
MedDRA Eye injuries NEC
HPO         Abnormality of the lens
Orphanet Abnormality of the eye
MedDRA Lens disorders congenital
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)
MedDRA:
Injury, poisoning and procedural complications(MedDRA:10022117)
    Injuries NEC(MedDRA:10022114)
       Eye injuries NEC(MedDRA:10027674)
          Ectopia lentis(HPO:0001083)
Congenital, familial and genetic disorders(MedDRA:10010331)
    Eye disorders congenital(MedDRA:10015920)
       Lens disorders congenital(MedDRA:10024205)
          Ectopia lentis(HPO:0001083)
Database Frequency: 45 / 7739
Resource:

All diseases associated with this symptom:

Aniridia (Orphanet:77)
Aniridia-intellectual deficit syndrome (Orphanet:1068)
Blepharoptosis - myopia - ectopia lentis (Orphanet:1259)
Classical homocystinuria (Orphanet:394)
Congenital contractural arachnodactyly (Orphanet:115)
Dyssegmental dysplasia, Rolland-Desbuquois type (Orphanet:156731)
ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE (OMIM:225100)
ECTOPIA LENTIS ET PUPILLAE (OMIM:225200)
Ectopia lentis - chorioretinal dystrophy - myopia (Orphanet:1884)
Ehlers-Danlos syndrome type 1 (Orphanet:90309)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Encephalopathy due to sulfite oxidase deficiency (Orphanet:833)
Epidermolysis bullosa simplex with anodontia/hypodontia (Orphanet:2325)
FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES,AND SPONTANEOUS FILTERING BLEBS (OMIM:601552)
Focal dermal hypoplasia (Orphanet:2092)
GLAUCOMA 3, PRIMARY CONGENITAL, D (OMIM:613086)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
Glaucoma secondary to spherophakia/ectopia lentis and megalocornea (Orphanet:238763)
Hyperlysinemia, type I (OMIM:238700)
Immunodeficiency by defective expression of HLA class 1 (Orphanet:34592)
Isolated ectopia lentis (Orphanet:1885)
Isolated sulfite oxidase deficiency (Orphanet:99731)
KNIEST-LIKE DYSPLASIA WITH PURSED LIPS AND ECTOPIA LENTIS (OMIM:245160)
Kniest dysplasia (Orphanet:485)
Knobloch syndrome (Orphanet:1571)
Leber congenital amaurosis 10 (OMIM:611755)
MARFANOID HYPERMOBILITY SYNDROME (OMIM:154750)
MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION (OMIM:614292)
Marfan syndrome (Orphanet:558)
Marfan syndrome type 1 (Orphanet:284963)
Marshall syndrome (Orphanet:560)
Microspherophakia - metaphyseal dysplasia (Orphanet:2551)
Norrie disease (Orphanet:649)
Oculofaciocardiodental syndrome (Orphanet:2712)
Schwartz-Jampel syndrome (Orphanet:800)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Stickler syndrome (Orphanet:828)
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A (Orphanet:308386)
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B (Orphanet:308393)
Temtamy syndrome (Orphanet:1777)
WEILL-MARCHESANI SYNDROME 1 (OMIM:277600)
WEILL-MARCHESANI SYNDROME 3 (OMIM:614819)
WEILL-MARCHESANI-LIKE SYNDROME (OMIM:613195)
Weill-Marchesani syndrome (Orphanet:3449)
Wildervanck syndrome (Orphanet:3456)