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 Acrocallosal Syndrome [C10.500.034.500] Acrocallosal Syndrome Aicardi Syndrome [C10.500.034.687] Aicardi Syndrome Holoprosencephaly [C10.500.034.875] Holoprosencephaly Septo-Optic Dysplasia [C10.500.034.937] Septo-Optic Dysplasia 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 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 Acrocallosal Syndrome [C16.131.666.034.500] Acrocallosal Syndrome Aicardi Syndrome [C16.131.666.034.687] Aicardi Syndrome Holoprosencephaly [C16.131.666.034.875] Holoprosencephaly Septo-Optic Dysplasia [C16.131.666.034.937] Septo-Optic Dysplasia 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 DISEASES Pathological Conditions, Signs and Symptoms [C23] Pathological Conditions, Signs and Symptoms Pathological Conditions, Anatomical [C23.300] Pathological Conditions, Anatomical Agenesis of Corpus Callosum [C23.300.008] Agenesis of Corpus Callosum Airway Remodeling [C23.300.017] Airway Remodeling Alopecia [C23.300.035] Alopecia Atrial Remodeling [C23.300.052] Atrial Remodeling Atrophy [C23.300.070] Atrophy Blister [C23.300.122] Blister Calculi [C23.300.175] Calculi Accessory Atrioventricular Bundle [C23.300.190] Accessory Atrioventricular Bundle Cerebral Cortical Thinning [C23.300.220] Cerebral Cortical Thinning Choristoma [C23.300.250] Choristoma Constriction, Pathologic [C23.300.287] Constriction, Pathologic Cysts [C23.300.306] Cysts Dilatation, Pathologic [C23.300.325] Dilatation, Pathologic Diverticulum [C23.300.415] Diverticulum Facial Asymmetry [C23.300.505] Facial Asymmetry Fistula [C23.300.575] Fistula Hernia [C23.300.707] Hernia Hypertrophy [C23.300.775] Hypertrophy Leg Length Inequality [C23.300.808] Leg Length Inequality Leukoplakia [C23.300.816] Leukoplakia Microvascular Rarefaction [C23.300.818] Microvascular Rarefaction Nails, Malformed [C23.300.820] Nails, Malformed Plaque, Amyloid [C23.300.821] Plaque, Amyloid Plaque, Atherosclerotic [C23.300.823] Plaque, Atherosclerotic Polyps [C23.300.825] Polyps Prolapse [C23.300.842] Prolapse Rupture, Spontaneous [C23.300.909] Rupture, Spontaneous Solitary Kidney [C23.300.925] Solitary Kidney Spontaneous Perforation [C23.300.940] Spontaneous Perforation Tertiary Lymphoid Structures [C23.300.955] Tertiary Lymphoid Structures Torsion Abnormality [C23.300.970] Torsion Abnormality Vascular Remodeling [C23.300.977] Vascular Remodeling Ventricular Remodeling [C23.300.985] Ventricular Remodeling

Agenesis of Corpus Callosum - Conceito preferido

Identificador do conceito	M0519523
Nota de escopo	Birth defect that results in a partial or complete absence of the CORPUS CALLOSUM. It may be isolated or a part of a syndrome (e.g., AICARDI'S SYNDROME; ACROCALLOSAL SYNDROME; ANDERMANN SYNDROME; and HOLOPROSENCEPHALY). Clinical manifestations include neuromotor skill impairment and INTELLECTUAL DISABILITY of variable severity.
Termo preferido	Agenesis of Corpus Callosum
Termo(s) alternativo(s)	Absence of Corpus Callosum Ageneses, Corpus Callosum Agenesis, Corpus Callosum Corpus Callosum Absence Corpus Callosum Absences Corpus Callosum Ageneses Corpus Callosum Agenesis Corpus Callosum Dysgeneses Corpus Callosum Dysgenesis Corpus Callosum Hypogeneses Corpus Callosum Hypogenesis Corpus Callosum, Agenesis Of Dysgeneses, Corpus Callosum Dysgenesis, Corpus Callosum Hypogeneses, Corpus Callosum Hypogenesis, Corpus Callosum

Corpus Callosum Malformation - Relacionado, mas não mais amplo ou mais específico

Identificador do conceito	M0556461
Termo preferido	Corpus Callosum Malformation