Disease Browser
Parent Node: Retinal Diseases (D012164) ..Starting node .. Retinal Perforations (D012167) Child Nodes:
Sister Nodes: ..Al Gazali Sabrinathan Nair syndrome (C535617) ..Angioid Streaks (D000793) ..Ausems Wittebol-Post Hennekam syndrome (C538272) ..Bestrophinopathy (C567518) ..BESTROPHINOPATHY, AUTOSOMAL RECESSIVE (OMIM:611809) ..Bietti Crystalline Dystrophy (C535440) ..Bothnia Retinal Dystrophy (C564392) ..Central Serous Chorioretinopathy (D056833) ..Cerebroretinal Microangiopathy with Calcifications and Cysts (C567401) ..Diabetic Retinopathy (D003930) 1 ..Epiretinal Membrane (D019773) ..Exudative Vitreoretinopathy 4 (C566619) ..Exudative Vitreoretinopathy 5 (C567648) ..Familial Exudative Vitreoretinopathy (C580083) ..Fleck Retina, Familial Benign (C565564) ..FLOTCH syndrome (C537065) ..Fundus Albipunctatus (C562733) ..Grouped Pigmentation of the Macula (C565530) ..Hypertensive Retinopathy (D058437) ..Iris hypoplasia and glaucoma (C535538) ..Leber Congenital Amaurosis (D057130) 20 ..Microcephaly with Chorioretinopathy, Autosomal Dominant (C563583) ..Microcephaly with Chorioretinopathy, Autosomal Recessive (C565379) ..MICROPHTHALMIA, ISOLATED 5 (OMIM:611040) ..Oculomelic amyoplasia (C537737) ..Rambaud Galian syndrome (C535283) ..Ramos Arroyo Clark syndrome (C535286) ..Retinal Aplasia (C566720) ..Retinal Artery Occlusion (D015356) 1 ..Retinal Degeneration (D012162) 195 ..Retinal Detachment (D012163) 9 ..Retinal Dysplasia (D015792) 2 ..RETINAL DYSPLASIA, PRIMARY (OMIM:312550) ..Retinal Hemorrhage (D012166) 2 ..Retinal Neoplasms (D019572) 3 ..Retinal Neovascularization (D015861) ..Retinal Nonattachment, Nonsyndromic Congenital (C565633) ..Retinal Perforations (D012167) ..Retinal Telangiectasis (D058456) 1 ..Retinal Vasculitis (D031300) 1 ..Retinal Vein Occlusion (D012170) ..Retinitis (D012173) 4 ..Retinopathy of Prematurity (D012178) ..Roifman syndrome (C535866) ..Stickler Syndrome, Autosomal Recessive, COL9A1-Related (C565177) ..Vasculopathy, Retinal, With Cerebral Leukodystrophy (C566007) ..Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia (C565179) ..Vitreoretinopathy, Proliferative (D018630) 5 Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 9731
Name: Retinal Perforations
Definition: Perforations through the whole thickness of the retina including the macula as the result of inflammation, trauma, degeneration, etc. The concept includes retinal breaks, tears, dialyses, and holes.
Alternative IDs:
ParentIDs: MESH:D012164
TreeNumbers: C11.768.740
Synonyms: Break, Retinal |Breaks, Retinal |Dialyses, Retinal |Hole, Macular |Hole, Retinal |Holes, Macular |Holes, Retinal |Macular Hole |Macular Holes |Perforation, Retinal |Perforations, Retinal |Retinal Break |Retinal Breaks |Retinal Dialyse |Retinal Dialyses |Retinal Hole |Re
Slim Mappings: Eye disease
Reference:
MedGen: D012167
MeSH: D012167
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants