Congenital anomaly of eye 19416009 SNOMED CT code SNOMED code 19416009 name Congenital anomaly of eye status active date introduced 2002-01-31 fully specified name(s) Congenital anomaly of eye (disorder) synonyms Congenital malformation of eye Congenital anomaly of eye Congenital deformity of eye Congenital abnormality of eye Congenital anomaly of the globe Congenital eye anomalies attributes - group1 Pathological process Pathological developmental process 308490002 Associated morphology Morphologically abnormal structure 49755003 Occurrence Congenital 255399007 Finding site Eye structure 81745001 parents children [X]Other specified congenital malformations of eye 205863004 removed: 2009-01-31 Acrorenoocular syndrome 720415006 Anophthalmia plus syndrome 720496006 Anophthalmos 7183006 Coloboma of eye 93390002 Colobomatous microphthalmia, rhizomelic dysplasia syndrome 764942005 Congenital anomaly of anterior segment of eye 429448005 Congenital anomaly of posterior segment of eye 128534003 Congenital anomaly of pupil 11211000119108 Congenital anomaly of sclera 32809005 Congenital cataracts, facial dysmorphism and neuropathy 702433001 Congenital disorders of eye and eyelid movements 230528000 removed: 2020-01-31 Congenital epibulbar choristoma of bilateral eyes 890378005 Congenital eye anomalies NOS 204222005 removed: 2010-01-31 Congenital malposition of eye 93320008 Congenital oculocutaneous hypopigmentation 61649007 Congenital orbit anomalies 204214003 removed: 2002-07-31 Cryptophthalmos syndrome 204102004 Deaf blind hypopigmentation syndrome Yemenite type 721084001 Duane's syndrome 60318001 Ectodermal dysplasia with blindness syndrome 721208007 Epibulbar lipodermoid, preauricular appendage, polythelia syndrome 1208480004 Hypoplasia of eye 86527000 Intractable diarrhea with choanal atresia and eye anomaly syndrome 720009004 Macrophthalmos 93181004 Matthew Wood syndrome 722458000 Melanosis oculi 45795007 Microcephaly, facial dysmorphism, ocular anomalies, multiple congenital anomalies syndrome 1279889005 Microphthalmia with brain and digit anomaly 721878003 Microphthalmos 61142002 Monophthalmos 92972001 Muscle eye brain disease with bilateral multicystic leukodystrophy 785298001 Ocular albinism 26399002 Oculoauricular syndrome Schorderet type 763815000 Oculocerebrofacial syndrome Kaufman type 722056009 Oculoskeletal dysplasia 699381006 Ophthalmo-acromelic syndrome 703403003 Orbital dystopia 253241005 Other eye anomalies NOS 204221003 removed: 2010-01-31 Other specified anterior segment anomalies 204167007 removed: 2010-01-31 Other specified eye anomalies 204220002 removed: 2010-01-31 Pierson syndrome 723449004 RAB18 deficiency 772225005 SOX2 anophthalmia syndrome 698851003 Triopia 1285322008 Upper limb defect with eye and ear abnormalities syndrome 716110002 White forelock with malformations syndrome 763619009 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 64572001 1279550006 371405004 11131000119108 19416009 138875005 404684003 118235002 128127008 127329003 19416009 138875005 404684003 64572001 118934005 87290003 19416009 ancestors sorted most to least specific
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