Retinal detachment
Symptom Information:
Symptom ID: | HPO:0000541 | |||||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||||||||||
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) MedDRA: Eye disorders(MedDRA:10015919) Ocular structural change, deposit and degeneration NEC(MedDRA:10042261) Retinal structural change, deposit and degeneration(MedDRA:10038896) Retinal detachment(HPO:0000541) |
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Database Frequency: | 87 / 7739 | |||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Adult-onset foveomacular vitelliform dystrophy | (Orphanet:99000) |
Aicardi syndrome | (Orphanet:50) |
Anti-glomerular basement membrane disease | (Orphanet:375) |
Autosomal dominant neovascular inflammatory vitreoretinopathy | (Orphanet:329211) |
Autosomal recessive chorioretinopathy-microcephaly | (Orphanet:2518) |
Brittle cornea syndrome | (Orphanet:90354) |
CATARACT 21, MULTIPLE TYPES | (OMIM:610202) |
CHARGE syndrome | (Orphanet:138) |
CONE DYSTROPHY, X-LINKED, WITH TAPETAL-LIKE SHEEN | (OMIM:304030) |
Classical homocystinuria | (Orphanet:394) |
Coats disease | (Orphanet:190) |
Cutis marmorata telangiectatica congenita | (Orphanet:1556) |
DWARFISM WITH STIFF JOINTS AND OCULAR ABNORMALITIES | (OMIM:127200) |
Deafness - epiphyseal dysplasia - short stature | (Orphanet:3218) |
Donnai-Barrow syndrome | (Orphanet:2143) |
ECTOPIA LENTIS ET PUPILLAE | (OMIM:225200) |
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 | (OMIM:601776) |
EXUDATIVE VITREORETINOPATHY 2, X-LINKED | (OMIM:305390) |
EXUDATIVE VITREORETINOPATHY 3 | (OMIM:605750) |
Ehlers-Danlos syndrome type 1 | (Orphanet:90309) |
Ehlers-Danlos syndrome type 2 | (Orphanet:90318) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Ehlers-Danlos syndrome, kyphoscoliotic type | (Orphanet:1900) |
Ehlers-Danlos syndrome, musculocontractural type | (Orphanet:2953) |
Familial exudative vitreoretinopathy | (Orphanet:891) |
Familial vascular leukoencephalopathy | (Orphanet:36383) |
Incontinentia pigmenti | (Orphanet:464) |
Isolated ectopia lentis | (Orphanet:1885) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
Kniest dysplasia | (Orphanet:485) |
Knobloch syndrome | (Orphanet:1571) |
LATTICE DEGENERATION OF RETINA LEADING TO RETINAL DETACHMENT | (OMIM:150500) |
MEGALOCORNEA | (OMIM:309300) |
MICROPHTHALMIA, ISOLATED 8 | (OMIM:615113) |
MICROSPHEROPHAKIA WITH HERNIA | (OMIM:157150) |
MRCS syndrome | (Orphanet:263347) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 | (OMIM:236670) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 11 | (OMIM:615181) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 | (OMIM:253800) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 5 | (OMIM:613153) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 7 | (OMIM:614643) |
MYOPIA 2, AUTOSOMAL DOMINANT | (OMIM:160700) |
MYOPIA 3, AUTOSOMAL DOMINANT | (OMIM:603221) |
MYOPIA 5, AUTOSOMAL DOMINANT | (OMIM:608474) |
MYOPIA, HIGH, WITH CATARACT AND VITREORETINAL DEGENERATION | (OMIM:614292) |
Marfan syndrome | (Orphanet:558) |
Marfan syndrome type 1 | (Orphanet:284963) |
Marfanoid syndrome, De Silva type | (Orphanet:2464) |
Marshall syndrome | (Orphanet:560) |
Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
Microspherophakia - metaphyseal dysplasia | (Orphanet:2551) |
Morning glory syndrome | (Orphanet:35737) |
Muscle-eye-brain disease | (Orphanet:588) |
Nance-Horan syndrome | (Orphanet:627) |
Norrie disease | (Orphanet:649) |
OPTIC DISC ANOMALIES WITH RETINAL AND/OR MACULAR DYSTROPHY | (OMIM:212550) |
Oculo-palato-cerebral syndrome | (Orphanet:2714) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Polyarteritis nodosa | (Orphanet:767) |
Progressive bifocal chorioretinal atrophy | (Orphanet:75373) |
Proteus syndrome | (Orphanet:744) |
Proteus-like syndrome | (Orphanet:2969) |
RETINAL DETACHMENT | (OMIM:180050) |
RETINAL DETACHMENT | (OMIM:312530) |
RETINAL DYSTROPHY AND OBESITY | (OMIM:616188) |
RETINITIS PIGMENTOSA 50 | (OMIM:613194) |
Renal coloboma syndrome | (Orphanet:1475) |
Retinopathy - anemia- central nervous system anomalies | (Orphanet:3088) |
SPONDYLOMEGAEPIPHYSEAL DYSPLASIA WITH UPPER LIMB MESOMELIA, PUNCTATECALCIFICATIONS, AND DEAFNESS | (OMIM:609616) |
STICKLER SYNDROME, TYPE I | (OMIM:108300) |
STICKLER SYNDROME, TYPE V | (OMIM:614284) |
Smith-Magenis syndrome | (Orphanet:819) |
Spondylo-ocular syndrome | (Orphanet:85194) |
Spondyloepimetaphyseal dysplasia congenita, Strudwick type | (Orphanet:93346) |
Spondyloepiphyseal dysplasia congenita | (Orphanet:94068) |
Spondyloepiphyseal dysplasia, MacDermot type | (Orphanet:163668) |
Stickler syndrome | (Orphanet:828) |
Stickler syndrome type 1 | (Orphanet:90653) |
Stickler syndrome type 2 | (Orphanet:90654) |
Stiff skin syndrome | (Orphanet:2833) |
Sturge-Weber syndrome | (Orphanet:3205) |
Uveal coloboma - cleft lip and palate - intellectual deficit | (Orphanet:1473) |
Vogt-Koyanagi-Harada disease | (Orphanet:3437) |
Von Hippel anomaly | (Orphanet:98941) |
Von Hippel-Lindau disease | (Orphanet:892) |
Walker-Warburg syndrome | (Orphanet:899) |
X-linked retinoschisis | (Orphanet:792) |