DISEASES Nervous System Diseases [C10] Nervous System Diseases Cranial Nerve Diseases [C10.292] Cranial Nerve Diseases Optic Nerve Diseases [C10.292.700] Optic Nerve Diseases Optic Atrophy [C10.292.700.225] Optic Atrophy Optic Disk Drusen [C10.292.700.450] Optic Disk Drusen Optic Nerve Hypoplasia [C10.292.700.463] Optic Nerve Hypoplasia Optic Nerve Injuries [C10.292.700.475] Optic Nerve Injuries Optic Nerve Neoplasms [C10.292.700.500] Optic Nerve Neoplasms Optic Neuritis [C10.292.700.550] Optic Neuritis Optic Neuropathy, Ischemic [C10.292.700.600] Optic Neuropathy, Ischemic Papilledema [C10.292.700.900] Papilledema DISEASES Nervous System Diseases [C10] Nervous System Diseases Nervous System Malformations [C10.500] Nervous System Malformations Agenesis of Corpus Callosum [C10.500.034] Agenesis of Corpus Callosum Central Nervous System Cysts [C10.500.142] Central Nervous System Cysts Central Nervous System Vascular Malformations [C10.500.190] Central Nervous System Vascular Malformations Congenital Cranial Dysinnervation Disorders [C10.500.198] Congenital Cranial Dysinnervation Disorders Dandy-Walker Syndrome [C10.500.205] Dandy-Walker Syndrome Hereditary Sensory and Autonomic Neuropathies [C10.500.250] Hereditary Sensory and Autonomic Neuropathies Hereditary Sensory and Motor Neuropathy [C10.500.300] Hereditary Sensory and Motor Neuropathy Hydranencephaly [C10.500.450] Hydranencephaly Malformations of Cortical Development [C10.500.507] Malformations of Cortical Development Neural Tube Defects [C10.500.680] Neural Tube Defects Optic Nerve Hypoplasia [C10.500.760] Optic Nerve Hypoplasia Septo-Optic Dysplasia [C10.500.760.500] Septo-Optic Dysplasia DISEASES Eye Diseases [C11] Eye Diseases Eye Diseases, Hereditary [C11.270] Eye Diseases, Hereditary Aicardi Syndrome [C11.270.019] Aicardi Syndrome Albinism [C11.270.040] Albinism Aniridia [C11.270.060] Aniridia Choroideremia [C11.270.142] Choroideremia Coloboma [C11.270.147] Coloboma Cone Dystrophy [C11.270.151] Cone Dystrophy Cone-Rod Dystrophies [C11.270.152] Cone-Rod Dystrophies Corneal Dystrophies, Hereditary [C11.270.162] Corneal Dystrophies, Hereditary Duane Retraction Syndrome [C11.270.235] Duane Retraction Syndrome Familial Exudative Vitreoretinopathies [C11.270.238] Familial Exudative Vitreoretinopathies Graves Ophthalmopathy [C11.270.240] Graves Ophthalmopathy Gyrate Atrophy [C11.270.468] Gyrate Atrophy Leber Congenital Amaurosis [C11.270.516] Leber Congenital Amaurosis Optic Atrophies, Hereditary [C11.270.564] Optic Atrophies, Hereditary Optic Nerve Hypoplasia [C11.270.588] Optic Nerve Hypoplasia Retinal Degeneration [C11.270.612] Retinal Degeneration Retinal Dysplasia [C11.270.660] Retinal Dysplasia Retinitis Pigmentosa [C11.270.684] Retinitis Pigmentosa Retinoblastoma [C11.270.862] Retinoblastoma Stargardt Disease [C11.270.872] Stargardt Disease Walker-Warburg Syndrome [C11.270.881] Walker-Warburg Syndrome Weill-Marchesani Syndrome [C11.270.921] Weill-Marchesani Syndrome DISEASES Eye Diseases [C11] Eye Diseases Optic Nerve Diseases [C11.640] Optic Nerve Diseases Low Tension Glaucoma [C11.640.225] Low Tension Glaucoma Optic Atrophy [C11.640.451] Optic Atrophy Optic Disk Drusen [C11.640.513] Optic Disk Drusen Optic Nerve Hypoplasia [C11.640.522] Optic Nerve Hypoplasia Optic Nerve Injuries [C11.640.530] Optic Nerve Injuries Optic Nerve Neoplasms [C11.640.544] Optic Nerve Neoplasms Optic Neuritis [C11.640.576] Optic Neuritis Optic Neuropathy, Ischemic [C11.640.643] Optic Neuropathy, Ischemic Papilledema [C11.640.710] Papilledema DISEASES Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormalities [C16.131] Congenital Abnormalities Nervous System Malformations [C16.131.666] Nervous System Malformations Agenesis of Corpus Callosum [C16.131.666.034] Agenesis of Corpus Callosum Central Nervous System Cysts [C16.131.666.142] Central Nervous System Cysts Central Nervous System Vascular Malformations [C16.131.666.190] Central Nervous System Vascular Malformations Congenital Cranial Dysinnervation Disorders [C16.131.666.198] Congenital Cranial Dysinnervation Disorders Dandy-Walker Syndrome [C16.131.666.205] Dandy-Walker Syndrome Hereditary Sensory and Motor Neuropathy [C16.131.666.300] Hereditary Sensory and Motor Neuropathy Hereditary Sensory and Autonomic Neuropathies [C16.131.666.310] Hereditary Sensory and Autonomic Neuropathies Hydranencephaly [C16.131.666.450] Hydranencephaly Malformations of Cortical Development [C16.131.666.507] Malformations of Cortical Development Neural Tube Defects [C16.131.666.680] Neural Tube Defects Optic Nerve Hypoplasia [C16.131.666.763] Optic Nerve Hypoplasia Septo-Optic Dysplasia [C16.131.666.763.500] Septo-Optic Dysplasia DISEASES Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] Congenital, Hereditary, and Neonatal Diseases and Abnormalities Genetic Diseases, Inborn [C16.320] Genetic Diseases, Inborn Eye Diseases, Hereditary [C16.320.290] Eye Diseases, Hereditary Aicardi Syndrome [C16.320.290.019] Aicardi Syndrome Albinism [C16.320.290.040] Albinism Aniridia [C16.320.290.078] Aniridia Choroideremia [C16.320.290.142] Choroideremia Cone-Rod Dystrophies [C16.320.290.152] Cone-Rod Dystrophies Corneal Dystrophies, Hereditary [C16.320.290.162] Corneal Dystrophies, Hereditary Duane Retraction Syndrome [C16.320.290.235] Duane Retraction Syndrome Familial Exudative Vitreoretinopathies [C16.320.290.352] Familial Exudative Vitreoretinopathies Graves Ophthalmopathy [C16.320.290.410] Graves Ophthalmopathy Gyrate Atrophy [C16.320.290.468] Gyrate Atrophy Optic Atrophies, Hereditary [C16.320.290.564] Optic Atrophies, Hereditary Optic Nerve Hypoplasia [C16.320.290.612] Optic Nerve Hypoplasia Retinal Dysplasia [C16.320.290.660] Retinal Dysplasia Retinitis Pigmentosa [C16.320.290.684] Retinitis Pigmentosa Stargardt Disease [C16.320.290.724] Stargardt Disease Vitelliform Macular Dystrophy [C16.320.290.763] Vitelliform Macular Dystrophy Weill-Marchesani Syndrome [C16.320.290.842] Weill-Marchesani Syndrome

Optic Nerve Hypoplasia - Concepto preferido

UI del concepto	M000647104
Nota de alcance	A group of rare genetic disorders characterized by underdeveloped OPTIC NERVES, resulting in increased incidences of vision impairment, CONGENITAL NYSTAGMUS and STRABISMUS. It may be syndromic, and is often associated with CNS malformations.
Término preferido	Optic Nerve Hypoplasia
Término(s) alternativo(s)	Hypoplasia, Optic Nerve

Superior Segmental Optic Nerve Hypoplasia - Más estrecho

UI del concepto	M000647105
Nota de alcance	Underdevelopment of the superior aspect of the OPTIC NERVE HEAD.
Término preferido	Superior Segmental Optic Nerve Hypoplasia
Término(s) alternativo(s)	Superior Segmental Optic Hypoplasia