Retinal detachment

Symptom Information:

Symptom ID: HPO:0000541
Synonyms:
Detached retina [HPO:0000541]
Retinal detachment (disorder) [Orphanet:5090]
Retinal Detachment [Orphanet:5090]
Detached retina [OMIM:Detached retina]
Retinal detachment [OMIM:Retinal detachment]
Retinal detachment [Orphanet:5090]
Retinal detachment [MedDRA:10038848]
Detached retina [MedDRA:10038848]
Detachment retinal [MedDRA:10038848]
Old retinal detachment, partial [MedDRA:10038848]
Old retinal detachment, total or subtotal [MedDRA:10038848]
Other forms of retinal detachment [MedDRA:10038848]
Other forms of retinal detachment not elsewhere classified [MedDRA:10038848]
Recent retinal detachment, partial, with giant tear [MedDRA:10038848]
Recent retinal detachment, partial, with multiple defects [MedDRA:10038848]
Recent retinal detachment, partial, with retinal dialysis [MedDRA:10038848]
Recent retinal detachment, partial, with single defect [MedDRA:10038848]
Recent retinal detachment, total or subtotal [MedDRA:10038848]
Retinal detachment with retinal defect [MedDRA:10038848]
Retinal detachment with retinal defect, unspecified [MedDRA:10038848]
Retinal detachments and defects [MedDRA:10038848]
Retinal detachments and defects, unspecified [MedDRA:10038848]
Serous retinal detachment [MedDRA:10038848]
Traction detachment of retina [MedDRA:10038848]
Unspecified retinal detachment [MedDRA:10038848]
Unspecified retinal detachments and defects [MedDRA:10038848]
Vitreoretinal detachment [MedDRA:10038848]
Amotio retinae [MedDRA:10038848]
Rhegmatogenous retinal detachment [MedDRA:10038848]
Subretinal fluid [MedDRA:10038848]
Detached retina (in some patients) [OMIM:Detached retina (in some patients)]
Retinal detachment (WWS) [OMIM:Retinal detachment (WWS)]
Retinal detachment (childhood) [OMIM:Retinal detachment (childhood)]
Retinal detachment (in 1 patient) [OMIM:Retinal detachment (in 1 patient)]
Retinal detachment (in some patients) [OMIM:Retinal detachment (in some patients)]
Retinal detachment (rare) [OMIM:Retinal detachment (rare)]
Retinal detachment (reported in 1 family) [OMIM:Retinal detachment (reported in 1 family)]
Quality:
Cross references:
HPO:0007899 "Retinal nonattachment" [Orphanet:5090]
Orphanet:5090 "Retinal detachment" [Orphanet:5090]
OMIM: "Detached retina" [OMIM:Detached retina]
OMIM: "Retinal detachment" [OMIM:Retinal detachment]
OMIM: "Detached retina (in some patients)" [OMIM:Detached retina (in some patients)]
OMIM: "Retinal detachment (WWS)" [OMIM:Retinal detachment (WWS)]
OMIM: "Retinal detachment (childhood)" [OMIM:Retinal detachment (childhood)]
OMIM: "Retinal detachment (in 1 patient)" [OMIM:Retinal detachment (in 1 patient)]
OMIM: "Retinal detachment (in some patients)" [OMIM:Retinal detachment (in some patients)]
OMIM: "Retinal detachment (rare)" [OMIM:Retinal detachment (rare)]
OMIM: "Retinal detachment (reported in 1 family)" [OMIM:Retinal detachment (reported in 1 family)]
UMLS:C0035305 "Retinal Detachment" [Orphanet:5090]
Is a (Direct Parents):
HPO         Abnormality of the retina
Orphanet Abnormality of the eye
MedDRA Retinal structural change, deposit and degeneration
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)
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)