Parent Terms |
Term With Siblings |
Child Terms |
|
angioid streaks of choroid
ataxia with oculomotor apraxia type 3
Ataxia-Microcephaly-Cataract Syndrome
ataxia-oculomotor apraxia type 4
Bietti crystalline corneoretinal dystrophy
Bothnia retinal dystrophy
Boucher-Neuhauser syndrome
cataract 17 multiple types
cataract 22 multiple types
Cavitary Optic Disc Anomalies
Cholestasis with Gallstone, Ataxia, and Visual Disturbance
congenital fibrosis of the extraocular muscles 1
congenital fibrosis of the extraocular muscles 2
congenital fibrosis of the extraocular muscles 3A
congenital fibrosis of the extraocular muscles 3C
congenital fibrosis of the extraocular muscles 5
dominant pericentral pigmentary retinopathy
Duane retraction syndrome +
dystrophies primarily involving the retinal pigment epithelium +
Encephalopathy with Intracranial Calcification, Growth Hormone Deficiency, Microcephaly, and Retinal Degeneration
exudative vitreoretinopathy +
familial benign fleck retina
Foveal Hypoplasia with Anterior Segment Anomalies
Ghose Sachdev Kumar Syndrome
Glaucoma 1, Open Angle, P
Grouped Pigmentation of the Macula
hereditary night blindness +
Hereditary Optic Atrophies +
hereditary retinal dystrophy +
hereditary spastic paraplegia 15
High Myopia with Cataract and Vitreoretinal Degeneration
Histiocytic Dermatoarthritis
Hyaloideoretinal Degeneration of Wagner
infantile cerebellar-retinal degeneration
Iris Pigment Epithelium Anomalies
late-onset retinal degeneration
Lattice Degeneration of Retina Leading to Retinal Detachment
Leber congenital amaurosis +
MacKay Shek Carr Syndrome
Microcephaly and Chorioretinopathy +
Microphthalmia with Hyperopia, Retinal Degeneration, Macrophakia, and Dental Anomalies
Myoectodermal Gonadal Dysgenesis Syndrome
Noble Bass Sherman Syndrome
Omphalocele, Diaphragmatic Hernia, and Radial Ray Defects
Ophthalmomandibulomelic Dysplasia
Peripapillary Atrophy, Beta Type
peripheral retinal degeneration +
Persistent Hyperplastic Primary Vitreous, Autosomal Dominant
Persistent Hyperplastic Primary Vitreous, Autosomal Recessive
pigmented paravenous chorioretinal atrophy
PORETTI-BOLTSHAUSER SYNDROME
primary congenital glaucoma +
Pseudoinflammatory Fundus Dystrophy, Finnish Type
Radial Drusen, Autosomal Dominant
renal hypomagnesemia 5 with ocular involvement
Reticular Dystrophy of Retinal Pigment Epithelium
Reticular Pigmentary Retinal Dystrophy of Posterior Pole
Retinal Degeneration and Epilepsy
Retinal Degeneration, Autosomal Recessive, Clumped Pigment Type
retinal dystrophies primarily involving Bruch's membrane
RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT
Retinal Dystrophy and Microvillus Inclusion Disease
Retinal Dystrophy and Obesity
retinal dystrophy in systemic or cerebroretinal lipidoses
RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES
RETINAL DYSTROPHY WITH OR WITHOUT EXTRAOCULAR ANOMALIES
Retinal Dystrophy with or without Macular Staphyloma
Retinal Dystrophy, Early Onset Severe +
Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome
Retinal Dystrophy, Juvenile Cataracts, and Short Stature Syndrome
Retinal Dystrophy, Optic Nerve Edema, Splenomegaly, Anhidrosis, and Migraine Headache Syndrome
retinitis pigmentosa + A retinal degeneration characterized by the gradual deterioration of the photoreceptors or the retinal pigment epithelium of the retina leading to progressive sight loss. (DO)
Retinohepatoendocrinologic Syndrome
Rhegmatogenous Retinal Detachment, Autosomal Dominant
snowflake vitreoretinal degeneration
Spondyloocular Syndrome, Autosomal Recessive
Stickler Syndrome, Type I, Nonsyndromic Ocular
Sveinsson chorioretinal atrophy
vitelliform macular dystrophy +
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia
Walker-Warburg syndrome +
Weill-Marchesani syndrome +
X-Linked Macular Dystrophy +
|
|
|
|