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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
cataract +     
3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia  
achromatopsia 4  
Achromatopsia 5  
Acrootoocular Syndrome 
Adams Nance Syndrome 
Aicardi syndrome 
Alacrima +   
Albinism +   
Alpha-B Crystallinopathy with Cataract 
aniridia +   
Aniridia 1  
Aniridia, Microcornea, and Spontaneously Reabsorbed Cataract 
Arachnodactyly Ataxia Cataract Aminoaciduria Mental Retardation 
ataxia with oculomotor apraxia type 3  
Ataxia-Microcephaly-Cataract Syndrome 
Ataxia-Oculomotor Apraxia 4  
Autosomal Recessive Nonsyndromic Congenital Nuclear Cataract 
Axonal Encephalopathy with Necrotizing Myopathy, Cardiomyopathy, and Cataracts 
Ayme-Gripp Syndrome  
basal laminar drusen  
Bassoe Syndrome 
bestrophinopathy  
Bhaskar Jagannathan Syndrome 
Bothnia retinal dystrophy  
bradyopsia  
CAHMR Syndrome 
CAMFAK Syndrome 
Capsule Opacification 
cataract 1 multiple types  
cataract 10 multiple types  
cataract 11 multiple types +   
cataract 12 multiple types  
cataract 13 with adult i phenotype  
cataract 14 multiple types  
cataract 15 multiple types  
cataract 16 multiple types  
cataract 17 multiple types  
cataract 18  
cataract 19 multiple types  
cataract 2 multiple types  
cataract 20 multiple types  
cataract 21 multiple types  
cataract 22 multiple types  
cataract 23  
cataract 24 
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
cataract 29 
cataract 3 multiple types  
cataract 30  
cataract 31 multiple types  
cataract 32 multiple types 
cataract 33  
cataract 34 multiple types  
cataract 35 
A cataract that has_material_basis_in variation in the region 19q13. (DO)
cataract 36  
cataract 37 
cataract 38  
cataract 39 multiple types  
cataract 4 multiple types +   
cataract 40  
cataract 41  
cataract 42  
cataract 43  
cataract 44  
cataract 45  
cataract 46 juvenile-onset  
Cataract 48  
cataract 5 multiple types  
cataract 6 multiple types  
cataract 7  
cataract 8 multiple types 
cataract 9 multiple types  
Cataract and Congenital Ichthyosis 
Cataract Ataxia Deafness 
Cataract Congenital Dominant Non Nuclear 
Cataract Hutterite Type  
Cataract Microcornea Syndrome  
Cataract, Age-Related Nuclear 
Cataract, Autosomal Dominant Nuclear  
Cataract, Autosomal Recessive Congenital 1 
Cataract, Cortical Pulverulent, Late-Onset 
Cataract, Crystalline Coralliform 
Cataract, Floriform 
Cataract, Lamellar 2  
Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome 
Cataract, Polymorphic and Lamellar 
Cataract, Posterior Polar, 5 
Cataract, Progressive Polymorphic Cortical 
Cataract, Pulverulent 
Cataract, Sutural, with Punctate and Cerulean Opacities  
Cataract, Variable Zonular Pulverulent 
Cataract, Zonular Central Nuclear 
Cataracts, Ataxia, Short Stature, and Mental Retardation 
CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA  
Cavitary Optic Disc Anomalies  
Cerebrooculofacioskeletal Syndrome 2  
Cerebrooculofacioskeletal Syndrome 4  
Cholestasis with Gallstone, Ataxia, and Visual Disturbance 
Choroideremia +   
Cochleosaccular Degeneration of the Inner Ear and Progressive Cataracts 
cone-rod dystrophy +   
Congenital Alacrima +   
Congenital Cataract with Mental Impairment and Dentate Gyrus Atrophy 
Congenital Cataracts, Facial Dysmorphism, and Neuropathy  
Congenital Cataracts, Hearing Loss, and Neurodegeneration  
Congenital Fibrosis of Extraocular Muscles, 2  
Congenital Fibrosis of Extraocular Muscles, 3A, with or without Extraocular Involvement  
Congenital Fibrosis of Extraocular Muscles, 3B  
Congenital Fibrosis of Extraocular Muscles, 3C 
Congenital Fibrosis of Extraocular Muscles, 5  
Congenital Infantile Muscular Dystrophy with Cataract and Hypogonadism 
congenital muscular dystrophy with cataracts and intellectual disability  
Congenital Mydriasis +   
Cornea Guttata with Anterior Polar Cataract 
Cornea Plana 1 
Cornea Plana 2  
corneal dystrophy +   
Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation 
Crome Syndrome 
Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly  
Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities 
diabetic cataract  
Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation 
Duane retraction syndrome +   
Edict Syndrome  
Enamel Hypoplasia, Cataracts, and Aqueductal Stenosis 
enhanced S-cone syndrome  
Fine-Lubinsky Syndrome 
Fleck Retina, Familial Benign  
Flynn Aird Syndrome 
Foveal Hypoplasia +   
Foveal Hypoplasia with Anterior Segment Anomalies  
Glaucoma 1, Open Angle, P  
Goldstein Hutt Syndrome 
Graves Ophthalmopathy  
Grouped Pigmentation of the Macula 
Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy 
gyrate atrophy +   
Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Cataracts  
hereditary night blindness +   
Hereditary Optic Atrophies +   
hereditary spastic paraplegia 9A  
high hyperopia  
Histiocytic Dermatoarthritis 
Hydrocephalus, Endocardial Fibroelastosis, and Cataracts 
hyperferritinemia-cataract syndrome  
Hypertrophic Neuropathy and Cataract 
hypomyelinating leukodystrophy 5  
Infantile Cataract, Skin Abnormalities, Glutamate Excess, and Impaired Intellectual Development  
Iris Pigment Epithelium Anomalies 
Isolated Microphthalmia with Cataract 1 
Isolated Microphthalmia with Cataract 2  
Isolated Microphthalmia with Cataract 3  
Isolated Microphthalmia with Cataract 4 
ITM2B-related cerebral amyloid angiopathy 2  
Joubert syndrome 8  
Juvenile Cataract, with Microcornea and Glucosuria  
Kahrizi syndrome  
Karandikar Maria Kamble Syndrome 
Kozlowski Rafinski Klicharska Syndrome 
Krasnow Qazi Syndrome 
Leber congenital amaurosis +   
Leg, Absence Deformity of, with Congenital Cataract 
Lipodystrophy with Congenital Cataracts and Neurodegeneration  
Lubinsky Syndrome 
Macular Dystrophy, X-Linked +   
Marinesco-Sjogren syndrome  
Marshall syndrome +   
Martsolf syndrome  
megalocornea +   
Microcephalic Primordial Dwarfism Toriello Type 
Microcephaly and Chorioretinopathy +   
Microcephaly, Cataracts, Impaired Intellectual Development, and Dystonia with Abnormal Striatum  
MICROCEPHALY, CONGENITAL CATARACT, AND PSORIASIFORM DERMATITIS  
Microcephaly, Growth Retardation, Cataract, Hearing Loss, and Unusual Appearance 
Microcephaly, Retinitis Pigmentosa, and Sutural Cataract 
Microphthalmia, Cataracts, and Iris Abnormalities  
Microphthalmia, Syndromic 2  
Mitochondrial Progressive Myopathy with Congenital Cataract, Hearing Loss, and Developmental Delay  
Mousa Al din Al Nassar Syndrome 
myofibrillar myopathy 2  
Myopathy, Cataract, Hypogonadism Syndrome 
Myopia, High, with Cataract and Vitreoretinal Degeneration  
myotonic cataract 
Nance-Horan syndrome  
Nathalie Syndrome 
NEURODEVELOPMENTAL DISORDER WITH CATARACTS, POOR GROWTH, AND DYSMORPHIC FACIES  
NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION  
NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CATARACTS, AND RENAL ABNORMALITIES  
O'Donnell Pappas Syndrome  
Oculoskeletodental Syndrome  
Omphalocele, Diaphragmatic Hernia, and Radial Ray Defects 
Ophthalmomandibulomelic Dysplasia 
optic atrophy 3  
Osteogenesis Imperfecta Congenita, Microcephaly, and Cataracts 
palmoplantar keratoderma and congenital alopecia 2 
Pavone Fiumara Rizzo Syndrome 
Peripapillary Atrophy, Beta Type 
Persistent Hyperplastic Primary Vitreous, Autosomal Dominant 
Persistent Hyperplastic Primary Vitreous, Autosomal Recessive  
Peters Anomaly with Cataract 
PHARC syndrome  
Pigmented Paravenous Chorioretinal Atrophy  
Polycystic Kidney, Cataract, and Congenital Blindness 
PORETTI-BOLTSHAUSER SYNDROME  
posterior polar cataract  
Premature Aging, Okamoto Type 
primary congenital glaucoma +   
pseudopapilledema 
Radial Drusen, Autosomal Dominant 
renal hypomagnesemia 5 with ocular involvement  
Retinal Aplasia 
Retinal Dysplasia +   
RETINAL DYSTROPHY AND IRIS COLOBOMA WITH OR WITHOUT CONGENITAL CATARACT  
Retinal Dystrophy, Early Onset Severe  
Retinal Dystrophy, Juvenile Cataracts, and Short Stature Syndrome  
retinitis pigmentosa +   
Retinohepatoendocrinologic Syndrome 
Rhegmatogenous Retinal Detachment, Autosomal Dominant  
Schaap Taylor Baraitser Syndrome 
Seemanova Lesny Syndrome 
Sengers syndrome  
senile cataract +   
Seow Najjar Syndrome 
Singh Chhaparwal Dhanda Syndrome 
Slavotinek Pike Mills Hurst Syndrome 
Spondyloepiphyseal Dysplasia with Coronal Craniosynostosis, Cataracts, Cleft Palate, and Mental Retardation 
Spondyloocular Syndrome, Autosomal Recessive  
Stickler Syndrome, Type I, Nonsyndromic Ocular  
tetanic cataract 
Vascular Hyalinosis 
Vici syndrome  
vitelliform macular dystrophy +   
Vitreoretinochoroidopathy  
Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia  
Walker-Warburg syndrome +   
Warburg micro syndrome +   
Weill-Marchesani syndrome +   
Wellesley Carmen French Syndrome 
Zonular Cataract and Nystagmus  

Synonyms
Exact Synonyms: CATCN1 ;   CTRCT35 ;   autosomal recessive congenital nuclear cataract 1 ;   cataract 35, congenital nuclear
Primary IDs: MESH:C563728 ;   RDO:0012913
Alternate IDs: OMIM:609376
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/15671291

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.