| Disease Browser
|
Parent Node:
 Eye Neoplasms (D005134) |
Parent Node:
Retinal Diseases (D012164) |
..Starting node
.. Retinal Neoplasms (D019572)
|
Child Nodes:
|
........Retinoblastoma (D012175)  2 |
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
|
