Disease Browser
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Parent Node: Cataract (D002386) |
..Starting node ..Cataract, Age-Related Nuclear (C563333)
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Child Nodes:
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Sister Nodes: |
..Absent corpus callosum cataract immunodeficiency (C535566)
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..Adams Nance syndrome (C538224)
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..Adult i Blood Group with Congenital Cataract (C566214)
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..Alpha-B Crystallinopathy (C563848)
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..Alpha-B Crystallinopathy with Cataract (C563849)
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..Aniridia, Microcornea, And Spontaneously Reabsorbed Cataract (C566280)
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..Anterior polar cataract 2 (C537774)
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..Arachnodactyly ataxia cataract aminoaciduria mental retardation (C537424)
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..Ataxia-Microcephaly-Cataract Syndrome (C563086)
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..Autosomal recessive nonsyndromic congenital nuclear cataract (C537298)
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..Bassoe syndrome (C537661)
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..Bhaskar Jagannathan syndrome (C535437)
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..CAHMR syndrome (C537959)
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..CAMFAK syndrome (C537965)
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..Capsule Opacification (D058442)
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..CATARACT 23 (OMIM:610425)
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..CATARACT 3, MULTIPLE TYPES (OMIM:601547)
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..CATARACT 32, MULTIPLE TYPES (OMIM:115650)
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..CATARACT 4, MULTIPLE TYPES (OMIM:115700)
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..CATARACT 6, MULTIPLE TYPES (OMIM:116600)
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..Cataract and cardiomyopathy (C538280)
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..Cataract and congenital ichthyosis (C538281)
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..Cataract anterior polar dominant (C538282)
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..Cataract ataxia deafness (C538283)
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..Cataract congenital dominant non nuclear (C538284)
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..Cataract congenital Volkmann type (C538285)
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..Cataract Hutterite type (C538286)
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..Cataract microcornea syndrome (C538287)
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..Cataract, Age-Related Cortical, 1 (C563812)
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..Cataract, Age-Related Cortical, 2 (C567814)
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..Cataract, Age-Related Nuclear (C563333)
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..Cataract, alopecia, sclerodactyly (C535336)
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..Cataract, Autosomal Dominant (C565815)
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..Cataract, Autosomal Dominant Nuclear (C565137)
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..Cataract, Autosomal Dominant, Multiple Types 1 (C566909)
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..Cataract, Autosomal Recessive Congenital 1 (C565136)
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..Cataract, autosomal recessive congenital 2 (C535337)
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..Cataract, Autosomal Recessive Congenital 3 (C567835)
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..Cataract, Autosomal Recessive, Early-Onset, Pulverulent (C565298)
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..Cataract, Central Saccular, With Sutural Opacities (C565301)
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..Cataract, Congenital Nuclear, Autosomal Recessive 1 (C563728)
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..Cataract, Congenital Nuclear, Autosomal Recessive 2 (C565725)
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..Cataract, Congenital Nuclear, Autosomal Recessive 3 (C566923)
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..CATARACT, CONGENITAL OR JUVENILE (OMIM:212500)
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..Cataract, Congenital Zonular, with Sutural Opacities (C563435)
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..Cataract, Congenital, Cerulean Type, 2 (C563294)
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..Cataract, Congenital, Cerulean Type, 3 (C563819)
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..Cataract, Congenital, with Mental Impairment and Dentate Gyrus Atrophy (C564353)
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..Cataract, congenital, with microcornea or slight microphthalmia (C535338)
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..Cataract, Coppock-Like (C565133)
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..Cataract, Cortical Pulverulent, Late-Onset (C563604)
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..Cataract, Cortical, Juvenile-Onset (C566955)
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..Cataract, Crystalline Aculeiform (C566162)
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..Cataract, Crystalline Coralliform (C566161)
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..Cataract, Floriform (C566160)
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..Cataract, Juvenile, With Microcornea And Glucosuria (C567434)
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..Cataract, Lamellar 2 (C566481)
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..Cataract, Microcephaly, Arthrogryposis, Kyphosis Syndrome (C566861)
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..Cataract, Nuclear Diffuse Nonprogressive (C566157)
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..Cataract, Nuclear Progressive (C564596)
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..Cataract, Nuclear Total (C566156)
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..Cataract, Polymorphic and Lamellar (C563603)
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..Cataract, posterior polar, 1 (C535339)
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..Cataract, Posterior Polar, 2 (C565134)
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..Cataract, posterior polar, 3 (C535343)
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..Cataract, posterior polar, 4 (C535344)
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..Cataract, posterior polar, 5 (C535340)
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..Cataract, Progressive Polymorphic Cortical (C565130)
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..Cataract, Pulverulent (C563426)
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..Cataract, Pulverulent, Juvenile-Onset (C565703)
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..Cataract, Punctate, Progressive Juvenile-Onset (C565131)
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..Cataract, Sutural, with Punctate and Cerulean Opacities (C564619)
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..Cataract, Variable Zonular Pulverulent (C565132)
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..Cataract, zonular (C535342)
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..Cataract, Zonular Central Nuclear (C565135)
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..Cataract, Zonular Pulverulent 1 (C566158)
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..Cataract, Zonular Pulverulent 3 (C566608)
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..Cataracts, ataxia, short stature, and mental retardation (C535345)
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..Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation (C563390)
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..Cerebrooculofacioskeletal Syndrome 2 (C565185)
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..Cerebrooculofacioskeletal Syndrome 4 (C565184)
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..Cerulean cataract (C537955)
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..Cochleosaccular degeneration of the inner ear and progressive cataracts (C536432)
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..Congenital Cataracts, Facial Dysmorphism, And Neuropathy (C565822)
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..Cornea guttata with anterior polar cataract (C535471)
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..Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation (C564271)
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..Crome syndrome (C536216)
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..Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly (C563840)
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..Deafness, Cataract, Retinitis Pigmentosa, And Sperm Abnormalities (C567467)
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..Dementia, familial Danish (C538209)
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..Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, And Mental Retardation (C566408)
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..Enamel Hypoplasia, Cataracts, and Aqueductal Stenosis (C563430)
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..Encephalopathy, Axonal, with Necrotizing Myopathy, Cardiomyopathy, and Cataracts (C565596)
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..Fine-Lubinsky syndrome (C537933)
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..Flynn Aird syndrome (C537066)
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..Goldstein Hutt syndrome (C537282)
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..Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy (C564264)
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..HEMORRHAGIC DESTRUCTION OF THE BRAIN, SUBEPENDYMAL CALCIFICATION, AND CATARACTS (OMIM:613730)
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..Hydrocephalus, endocardial fibroelastosis, and cataracts (C535855)
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..Hyperferritinemia, hereditary, with congenital cataracts (C538137)
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..Hypertrophic Neuropathy And Cataract (C565490)
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..Kahrizi Syndrome (C567196)
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..Karandikar Maria Kamble syndrome (C537009)
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..Kozlowski Rafinski Klicharska syndrome (C537509)
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..Krasnow Qazi syndrome (C537616)
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..Leg, Absence Deformity of, with Congenital Cataract (C565442)
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..Leukodystrophy, Hypomyelinating, 5 (C567166)
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..Lipodystrophy with Congenital Cataracts and Neurodegeneration (C564669)
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..Lubinsky syndrome (C543092)
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..Marinesco-Sjogren-like syndrome (MSLS) (C535913)
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..Marshall syndrome (C536025)
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..Martsolf syndrome (C536028)
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..Microcephalic primordial dwarfism Toriello type (C537321)
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..Microcephaly, Growth Retardation, Cataract, Hearing Loss, And Unusual Appearance (C567849)
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..Microcephaly, Retinitis Pigmentosa, and Sutural Cataract (C563296)
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..Microphthalmia, Cataracts, and Iris Abnormalities (C566448)
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..Microphthalmia, Isolated, with Cataract 1 (C563582)
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..Microphthalmia, Isolated, with Cataract 2 (C565876)
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..Microphthalmia, Isolated, with Cataract 3 (C564452)
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..Microphthalmia, Isolated, with Cataract 4 (C566480)
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..Microphthalmia, syndromic 2 (C537465)
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..Mousa Al din Al Nassar syndrome (C536989)
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..Muscular dystrophy, congenital, infantile with cataract and hypogonadism (C537385)
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..Myopathy, Cataract, Hypogonadism Syndrome (C563578)
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..Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay (C567769)
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..Nance-Horan syndrome (C538336)
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..Nathalie syndrome (C538342)
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..O'Donnell Pappas syndrome (C537858)
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..Optic atrophy and cataract, autosomal dominant (C537128)
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..Osteogenesis imperfecta congenita, microcephaly, and cataracts (C537558)
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..Pavone Fiumara Rizzo syndrome (C536313)
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..Peters anomaly with cataract (C537885)
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..Polycystic Kidney, Cataract, and Congenital Blindness (C564882)
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..Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract (C567203)
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..Premature aging, Okamoto type (C535270)
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..Schaap Taylor Baraitser syndrome (C536626)
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..Seemanova Lesny syndrome (C537536)
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..Seow Najjar syndrome (C537584)
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..Singh Chhaparwal Dhanda syndrome (C537341)
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..Slavotinek Pike Mills Hurst syndrome (C536672)
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..Spastic paraplegia 9, autosomal dominant (C536868)
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..Spondyloepiphyseal Dysplasia With Coronal Craniosynostosis, Cataracts, Cleft Palate, And Mental Retardation (C566515)
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..Spondyloocular Syndrome, Autosomal Recessive (C565285)
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..Warburg Sjo Fledelius syndrome (C536681)
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..Wellesley Carmen French syndrome (C536691)
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..Zonular cataract and nystagmus (C536727)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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