| Disease Browser
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Parent Node:
 Blepharitis (D001762) |
Parent Node:
Epidermal Cyst (D004814) |
Parent Node:
Hair Diseases (D006201) |
Parent Node:
Nail Diseases (D009260) |
Parent Node:
Pigmentation Disorders (D010859) |
Parent Node:
Retinal Diseases (D012164) |
..Starting node
.. FLOTCH syndrome (C537065)
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Child Nodes:
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Sister Nodes: |
..Al Gazali Sabrinathan Nair syndrome (C535617)
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..Angioid Streaks (D000793)
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..Ausems Wittebol-Post Hennekam syndrome (C538272)
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..Bestrophinopathy (C567518)
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..BESTROPHINOPATHY, AUTOSOMAL RECESSIVE (OMIM:611809)
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..Bietti Crystalline Dystrophy (C535440)
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..Bothnia Retinal Dystrophy (C564392)
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..Central Serous Chorioretinopathy (D056833)
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..Cerebroretinal Microangiopathy with Calcifications and Cysts (C567401)
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..Diabetic Retinopathy (D003930)  1
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..Epiretinal Membrane (D019773)
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..Exudative Vitreoretinopathy 4 (C566619)
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..Exudative Vitreoretinopathy 5 (C567648)
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..Familial Exudative Vitreoretinopathy (C580083)
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..Fleck Retina, Familial Benign (C565564)
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..FLOTCH syndrome (C537065)
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..Fundus Albipunctatus (C562733)
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..Grouped Pigmentation of the Macula (C565530)
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..Hypertensive Retinopathy (D058437)
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..Iris hypoplasia and glaucoma (C535538)
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..Leber Congenital Amaurosis (D057130) 20
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..Microcephaly with Chorioretinopathy, Autosomal Dominant (C563583)
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..Microcephaly with Chorioretinopathy, Autosomal Recessive (C565379)
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..MICROPHTHALMIA, ISOLATED 5 (OMIM:611040)
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..Oculomelic amyoplasia (C537737)
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..Rambaud Galian syndrome (C535283)
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..Ramos Arroyo Clark syndrome (C535286)
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..Retinal Aplasia (C566720)
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..Retinal Artery Occlusion (D015356) 1
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..Retinal Degeneration (D012162) 195
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..Retinal Detachment (D012163) 9
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..Retinal Dysplasia (D015792) 2
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..RETINAL DYSPLASIA, PRIMARY (OMIM:312550)
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..Retinal Hemorrhage (D012166) 2
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..Retinal Neoplasms (D019572) 3
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..Retinal Neovascularization (D015861)
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..Retinal Nonattachment, Nonsyndromic Congenital (C565633)
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..Retinal Perforations (D012167)
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..Retinal Telangiectasis (D058456) 1
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..Retinal Vasculitis (D031300) 1
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..Retinal Vein Occlusion (D012170)
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..Retinitis (D012173) 4
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..Retinopathy of Prematurity (D012178)
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..Roifman syndrome (C535866)
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..Stickler Syndrome, Autosomal Recessive, COL9A1-Related (C565177)
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..Vasculopathy, Retinal, With Cerebral Leukodystrophy (C566007)
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..Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia (C565179)
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..Vitreoretinopathy, Proliferative (D018630) 5
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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