OMOP Concept 4027702
Congenital anomaly of lens
StandardConditionSNOMED128353007Disorder
Maps from
23
Descendants
115
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
23 source codes normalize to Congenital anomaly of lens via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Congenital anomaly of lens across source vocabularies.
- anomalía congénita del cristalino
- anomalía congénita del cristalino (trastorno)
- Congenital anomaly of lens (disorder)
- Congenital lens anomaly
- Congenital malformation of lens
- malformación congénita del cristalino
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(25)Roll up to these when you need a wider cohort.
- 1Congenital anomaly of anterior segment of eye
- 1Disorder of lens
- 2Congenital anomaly of eye
- 2Crystalline lens finding
- 2Disorder of anterior segment of eye
- 3Anomaly of eye
- 3Anterior segment finding
- 3Congenital anomaly of head
- 3Congenital anomaly of visual system
- 3Disorder of eye
- 4Congenital malformation
- 4Disorder of eye region
- 4Disorder of head
- 4Disorder of sensory organ
- 4Globe finding
- 4Visual system disorder
- 5Congenital disease
- 5Developmental disorder
- 5Disease
- 5Disorder of body system
- 5Eye / vision finding
- 5Finding of head region
- 5Head finding
- 6Clinical finding
- 6Disorder of fetus and/or newborn
Narrower concepts
(115)Included automatically when you query with descendants.
- 1Coloboma of lens
- 1Congenital anomaly of lens shape
- 1Congenital anomaly of zonula
- 1Congenital aphakia
- 1Congenital cataract
- 1Congenital ectopic lens
- 1Congenital pigmentation of lens
- 1Ectopia lentis et pupillae
- 1Facial dysmorphism, lens dislocation, anterior segment abnormalities, spontaneous filtering bleb syndrome
- 1Microphakia
- 1Persistent tunica vasculosa lentis
- 2Absence deformity of leg and congenital cataract syndrome
- 2Bilateral primary aphakia
- 2Blepharoptosis, myopia, ectopia lentis syndrome
- 2Cataract and microcornea syndrome
- 2Cataract, congenital heart disease, neural tube defect syndrome
- 2Congenital anterior capsular pigmentation
- 2Congenital aphakia, iris hypoplasia, microphthalmia, microcornea syndrome
- 2Congenital capsular cataract
- 2Congenital cataract, hearing loss, severe developmental delay syndrome
- 2Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome
- 2Congenital cataract ichthyosis syndrome
- 2Congenital cataract microcornea with corneal opacity
- 2Congenital cataract of left eye
- 2Congenital cataract of right eye
- 2Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome
- 2Congenital cataract, severe neonatal hepatopathy, global developmental delay syndrome
- 2Congenital cataract with ataxia and deafness syndrome
- 2Congenital cataract with deafness and hypogonadism syndrome
- 2Congenital cataract with hypertrichosis and intellectual disability syndrome
- 2Congenital coloboma of left lens
- 2Congenital coloboma of right lens
- 2Congenital combined form cataract
- 2Congenital cortical cataract
- 2Congenital membranous cataract
- 2Congenital polar cataract
- 2Congenital subcapsular cataract
- 2Congenital total cataract
- 2Congenital zonular cataract
- 2Coralliform cataract
- 2Cortical and zonular cataract
- 2Crome syndrome
- 2Ectopia lentis, chorioretinal dystrophy, myopia syndrome
- 2Embryonal nuclear cataract
- 2Exacerbation of congenital cataract
- 2Hutterite type cataract
- 2Hydrocephalus with endocardial fibroelastosis and cataract syndrome
- 2Hypergonadotropic hypogonadism with cataract syndrome
- 2Intellectual disability, cataract, calcified pinna, myopathy syndrome
- 2Karandikar Maria Kamble syndrome
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