Ectopia lentis
Symptom Information:
Symptom ID: | HPO:0001083 | |||||||||||||||||||||||||||||||||||
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 lens(HPO:0000517) Ectopia lentis(HPO:0001083) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Eye disorders congenital(MedDRA:10015920) Lens disorders congenital(MedDRA:10024205) Ectopia lentis(HPO:0001083) Injury, poisoning and procedural complications(MedDRA:10022117) Injuries NEC(MedDRA:10022114) Eye injuries NEC(MedDRA:10027674) Ectopia lentis(HPO:0001083) |
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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) |