Retinal nonattachment
Symptom Information:
Symptom ID: | HPO:0007899 | ||||||||||||||||||||||||||||||||||||
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 posterior segment of the globe(HPO:0004329) Abnormality of the fundus(HPO:0001098) Abnormality of the retina(HPO:0000479) Retinal detachment(HPO:0000541) Retinal nonattachment(HPO:0007899) MedDRA: Eye disorders(MedDRA:10015919) Ocular structural change, deposit and degeneration NEC(MedDRA:10042261) Retinal structural change, deposit and degeneration(MedDRA:10038896) Retinal nonattachment(HPO:0007899) |
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Database Frequency: | 10 / 7739 | ||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Congenital blindness due to retinal non-attachment | (Orphanet:300337) |
ECTOPIA LENTIS ET PUPILLAE | (OMIM:225200) |
Familial vascular leukoencephalopathy | (Orphanet:36383) |
Knobloch syndrome | (Orphanet:1571) |
MICROPHTHALMIA, ISOLATED 8 | (OMIM:615113) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 | (OMIM:236670) |
MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION | (OMIM:614292) |
RETINAL NONATTACHMENT AND FALCIFORM DETACHMENT | (OMIM:180070) |
Renal coloboma syndrome | (Orphanet:1475) |
Spondyloepiphyseal dysplasia, MacDermot type | (Orphanet:163668) |