| Disease Browser
|
Parent Node:
 Cataract (D002386) |
Parent Node:
Eye Diseases, Hereditary (D015785) |
..Starting node
.. Cataract, Pulverulent (C563426)
|
Child Nodes:
|
Sister Nodes: |
..Achromatopsia 4 (C564206)
|
..Achromatopsia 5 (C567759)
|
..Acrootoocular Syndrome (C564866)
|
..Aicardi Syndrome (D058540)  1
|
..Alacrima (C562827)
|
..Alacrima, Congenital (C566307)
|
..Albinism (D000417) 30
|
..Aniridia (D015783) 10
|
..Ataxia-Microcephaly-Cataract Syndrome (C563086)
|
..Basal Laminar Drusen (C563034)
|
..Bestrophinopathy (C567518)
|
..Bothnia Retinal Dystrophy (C564392)
|
..Cataract, Congenital Nuclear, Autosomal Recessive 1 (C563728)
|
..Cataract, Congenital Nuclear, Autosomal Recessive 2 (C565725)
|
..Cataract, Congenital Nuclear, Autosomal Recessive 3 (C566923)
|
..Cataract, Floriform (C566160)
|
..Cataract, Pulverulent (C563426)
|
..Cavitary Optic Disc Anomalies (C566924)
|
..Cholestasis with Gallstone, Ataxia, and Visual Disturbance (C565856)
|
..Choroideremia (D015794) 2
|
..Congenital Fibrosis of the Extraocular Muscles (C580012)
|
..Cornea Plana 1 (C565158)
|
..Cornea Plana 2 (C565677)
|
..Corneal Dystrophies, Hereditary (D003317) 61
|
..CSNB1C (C567704)
|
..Drusen, Radial, Autosomal Dominant (C565088)
|
..Duane Retraction Syndrome (D004370) 2
|
..Enhanced S-Cone Syndrome (C564835)
|
..Fibrosis Of Extraocular Muscles, Congenital, 2 (C566587)
|
..Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement (C567572)
|
..Fibrosis of Extraocular Muscles, Congenital, 3B (C567739)
|
..Fibrosis of Extraocular Muscles, Congenital, 3C (C567666)
|
..Fleck Retina, Familial Benign (C565564)
|
..Foveal Hypoplasia with Anterior Segment Anomalies (C565006)
|
..Foveal Hypoplasia, Isolated (C565005)
|
..Graves Ophthalmopathy (D049970)
|
..Grouped Pigmentation of the Macula (C565530)
|
..Gyrate Atrophy (D015799) 1
|
..Histiocytic Dermatoarthritis (C564183)
|
..Hyperopia, High (C565497)
|
..Hypomagnesemia 5, Renal, with Ocular Involvement (C565423)
|
..Iris Pigment Epithelium Anomalies (C566651)
|
..Joubert Syndrome 8 (C567358)
|
..Leber Congenital Amaurosis (D057130) 20
|
..Macular Dystrophy, X-Linked (C564110)
|
..Megalocornea (C562829)
|
..Microcephaly with Chorioretinopathy, Autosomal Recessive (C565379)
|
..Mydriasis, Congenital (C563221)
|
..Night blindness, congenital stationary (C536122) 4
|
..Night Blindness, Congenital Stationary, Autosomal Dominant 1 (C566474)
|
..Night Blindness, Congenital Stationary, Autosomal Dominant 2 (C566869)
|
..Night Blindness, Congenital Stationary, Autosomal Dominant 3 (C566475)
|
..Omphalocele, Diaphragmatic Hernia, And Radial Ray Defects (C563701)
|
..Ophthalmomandibulomelic Dysplasia (C563501)
|
..Optic Atrophies, Hereditary (D015418) 30
|
..Peripapillary Atrophy, Beta Type (C566898)
|
..Persistent Hyperplastic Primary Vitreous, Autosomal Recessive (C566966)
|
..Pigmented Paravenous Chorioretinal Atrophy (C566801)
|
..Prolonged Electroretinal Response Suppression (C564243)
|
..Pseudoglaucoma (C566748)
|
..Pseudopapilledema (C562401)
|
..Retinal Aplasia (C566720)
|
..Retinal Dysplasia (D015792) 2
|
..Retinal Dystrophy, Early Onset Severe (C565741)
|
..Retinitis Pigmentosa (D012174) 132
|
..Retinohepatoendocrinologic Syndrome (C564839)
|
..Rhegmatogenous Retinal Detachment, Autosomal Dominant (C563710)
|
..Spondyloocular Syndrome, Autosomal Recessive (C565285)
|
..Stickler Syndrome, Type I, Nonsyndromic Ocular (C563709)
|
..Vascular Hyalinosis (C564750)
|
..Vitelliform Macular Dystrophy (D057826) 2
|
..Vitreoretinochoroidopathy (C536352)
|
..Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia (C565179)
|
..Walker-Warburg Syndrome (D058494) 7
|
..Weill-Marchesani Syndrome (D056846)
|
..Weill-Marchesani-Like Syndrome (C567710)
|
Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
|
