Retinal nonattachment

Symptom Information:

Symptom ID: HPO:0007899
Synonyms:
Congenital retinal non-attachment [HPO:0007899]
Retinal detachment [Orphanet:5090]
Retinal detachment (disorder) [Orphanet:5090]
Retinal Detachment [Orphanet:5090]
Congenital retinal non-attachment [OMIM:Congenital retinal non-attachment]
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:0000541 "Retinal detachment" [Orphanet:5090]
Orphanet:5090 "Retinal detachment" [Orphanet:5090]
OMIM: "Congenital retinal non-attachment" [OMIM:Congenital retinal non-attachment]
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):
MedDRA Retinal structural change, deposit and degeneration
Orphanet Abnormality of the eye
HPO         Retinal detachment
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)
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)