DISEASES Nervous System Diseases [C10] Nervous System Diseases Autoimmune Diseases of the Nervous System [C10.114] Autoimmune Diseases of the Nervous System Autonomic Nervous System Diseases [C10.177] Autonomic Nervous System Diseases Central Nervous System Diseases [C10.228] Central Nervous System Diseases Chronobiology Disorders [C10.281] Chronobiology Disorders Cranial Nerve Diseases [C10.292] Cranial Nerve Diseases Demyelinating Diseases [C10.314] Demyelinating 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 Nervous System Neoplasms [C10.551] Nervous System Neoplasms Neurocutaneous Syndromes [C10.562] Neurocutaneous Syndromes Neurodegenerative Diseases [C10.574] Neurodegenerative Diseases Neuroinflammatory Diseases [C10.586] Neuroinflammatory Diseases Neurologic Manifestations [C10.597] Neurologic Manifestations Neuromuscular Diseases [C10.668] Neuromuscular Diseases Neurotoxicity Syndromes [C10.720] Neurotoxicity Syndromes Restless Legs Syndrome [C10.803] Restless Legs Syndrome Sleep Wake Disorders [C10.886] Sleep Wake Disorders Trauma, Nervous System [C10.900] Trauma, Nervous System DISEASES Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormalities [C16.131] Congenital Abnormalities Abnormalities, Drug-Induced [C16.131.042] Abnormalities, Drug-Induced Abnormalities, Multiple [C16.131.077] Abnormalities, Multiple Abnormalities, Radiation-Induced [C16.131.080] Abnormalities, Radiation-Induced Abnormalities, Severe Teratoid [C16.131.085] Abnormalities, Severe Teratoid Aicardi Syndrome [C16.131.162] Aicardi Syndrome Cardiovascular Abnormalities [C16.131.240] Cardiovascular Abnormalities Chromosome Disorders [C16.131.260] Chromosome Disorders Congenital Microtia [C16.131.287] Congenital Microtia Digestive System Abnormalities [C16.131.314] Digestive System Abnormalities Eye Abnormalities [C16.131.384] Eye Abnormalities Hernias, Diaphragmatic, Congenital [C16.131.433] Hernias, Diaphragmatic, Congenital Lymphatic Abnormalities [C16.131.482] Lymphatic Abnormalities Musculoskeletal Abnormalities [C16.131.621] Musculoskeletal 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 Respiratory System Abnormalities [C16.131.740] Respiratory System Abnormalities Situs Inversus [C16.131.810] Situs Inversus Skin Abnormalities [C16.131.831] Skin Abnormalities Stomatognathic System Abnormalities [C16.131.850] Stomatognathic System Abnormalities Thyroid Dysgenesis [C16.131.894] Thyroid Dysgenesis Urogenital Abnormalities [C16.131.939] Urogenital Abnormalities

Nervous System Malformations - Concepto preferido

UI del concepto	M0014666
Nota de alcance	Structural abnormalities of the central or peripheral nervous system resulting primarily from defects of embryogenesis.
Término preferido	Nervous System Malformations
Término(s) alternativo(s)	Abnormalities, Congenital, Nervous System Abnormalities, Nervous System Abnormality, Nervous System Anomalies, Nervous System Anomaly, Nervous System Congenital Abnormalities, Nervous System Congenital Anomalies, Nervous System Congenital Malformations, Nervous System Malformation, Nervous System Malformations, Nervous System Malformations, Nervous System, Congenital Nervous System Abnormalities Nervous System Abnormality Nervous System Anomalies Nervous System Anomaly Nervous System Congenital Abnormalities Nervous System Congenital Malformations Nervous System Malformation Nervous System Malformations, Congenital

Cranioschisis - Más estrecho

UI del concepto	M0333688
Término preferido	Cranioschisis
Término(s) alternativo(s)	Cranioschises