DISEASES Stomatognathic Diseases [C07] Stomatognathic Diseases Mouth Diseases [C07.465] Mouth Diseases Facial Nerve Diseases [C07.465.299] Facial Nerve Diseases Bell Palsy [C07.465.299.250] Bell Palsy Facial Hemiatrophy [C07.465.299.375] Facial Hemiatrophy Facial Nerve Injuries [C07.465.299.500] Facial Nerve Injuries Facial Neuralgia [C07.465.299.625] Facial Neuralgia Herpes Zoster Oticus [C07.465.299.750] Herpes Zoster Oticus Melkersson-Rosenthal Syndrome [C07.465.299.800] Melkersson-Rosenthal Syndrome Mobius Syndrome [C07.465.299.825] Mobius Syndrome DISEASES Nervous System Diseases [C10] Nervous System Diseases Cranial Nerve Diseases [C10.292] Cranial Nerve Diseases Facial Nerve Diseases [C10.292.319] Facial Nerve Diseases Bell Palsy [C10.292.319.250] Bell Palsy Facial Hemiatrophy [C10.292.319.375] Facial Hemiatrophy Facial Nerve Injuries [C10.292.319.500] Facial Nerve Injuries Facial Neuralgia [C10.292.319.625] Facial Neuralgia Herpes Zoster Oticus [C10.292.319.750] Herpes Zoster Oticus Melkersson-Rosenthal Syndrome [C10.292.319.800] Melkersson-Rosenthal Syndrome Mobius Syndrome [C10.292.319.825] Mobius Syndrome DISEASES Nervous System Diseases [C10] Nervous System Diseases Cranial Nerve Diseases [C10.292] Cranial Nerve Diseases Ocular Motility Disorders [C10.292.562] Ocular Motility Disorders Oculomotor Nerve Diseases [C10.292.562.700] Oculomotor Nerve Diseases Congenital Cranial Dysinnervation Disorders [C10.292.562.700.375] Congenital Cranial Dysinnervation Disorders Duane Retraction Syndrome [C10.292.562.700.375.500] Duane Retraction Syndrome Mobius Syndrome [C10.292.562.700.375.750] Mobius Syndrome Septo-Optic Dysplasia [C10.292.562.700.375.875] Septo-Optic Dysplasia DISEASES Eye Diseases [C11] Eye Diseases Ocular Motility Disorders [C11.590] Ocular Motility Disorders Oculomotor Nerve Diseases [C11.590.436] Oculomotor Nerve Diseases Congenital Cranial Dysinnervation Disorders [C11.590.436.400] Congenital Cranial Dysinnervation Disorders Duane Retraction Syndrome [C11.590.436.400.500] Duane Retraction Syndrome Mobius Syndrome [C11.590.436.400.750] Mobius Syndrome Septo-Optic Dysplasia [C11.590.436.400.875] Septo-Optic Dysplasia DISEASES Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormalities [C16.131] Congenital Abnormalities Abnormalities, Multiple [C16.131.077] Abnormalities, Multiple 22q11 Deletion Syndrome [C16.131.077.019] 22q11 Deletion Syndrome Alagille Syndrome [C16.131.077.065] Alagille Syndrome Angelman Syndrome [C16.131.077.095] Angelman Syndrome Barth Syndrome [C16.131.077.121] Barth Syndrome Basal Cell Nevus Syndrome [C16.131.077.130] Basal Cell Nevus Syndrome Beckwith-Wiedemann Syndrome [C16.131.077.133] Beckwith-Wiedemann Syndrome Bloom Syndrome [C16.131.077.137] Bloom Syndrome Branchio-Oto-Renal Syndrome [C16.131.077.208] Branchio-Oto-Renal Syndrome Carney Complex [C16.131.077.229] Carney Complex Ciliopathies [C16.131.077.245] Ciliopathies Cockayne Syndrome [C16.131.077.250] Cockayne Syndrome Costello Syndrome [C16.131.077.256] Costello Syndrome Cri-du-Chat Syndrome [C16.131.077.262] Cri-du-Chat Syndrome De Lange Syndrome [C16.131.077.272] De Lange Syndrome Deaf-Blind Disorders [C16.131.077.299] Deaf-Blind Disorders Donohue Syndrome [C16.131.077.313] Donohue Syndrome Down Syndrome [C16.131.077.327] Down Syndrome Ectodermal Dysplasia [C16.131.077.350] Ectodermal Dysplasia Fraser Syndrome [C16.131.077.371] Fraser Syndrome Gardner Syndrome [C16.131.077.393] Gardner Syndrome Heterotaxy Syndrome [C16.131.077.401] Heterotaxy Syndrome Holoprosencephaly [C16.131.077.410] Holoprosencephaly Incontinentia Pigmenti [C16.131.077.445] Incontinentia Pigmenti Isolated Noncompaction of the Ventricular Myocardium [C16.131.077.477] Isolated Noncompaction of the Ventricular Myocardium Laurence-Moon Syndrome [C16.131.077.509] Laurence-Moon Syndrome LEOPARD Syndrome [C16.131.077.525] LEOPARD Syndrome Loeys-Dietz Syndrome [C16.131.077.537] Loeys-Dietz Syndrome Marfan Syndrome [C16.131.077.550] Marfan Syndrome Mobius Syndrome [C16.131.077.578] Mobius Syndrome Monilethrix [C16.131.077.592] Monilethrix Nail-Patella Syndrome [C16.131.077.606] Nail-Patella Syndrome Netherton Syndrome [C16.131.077.619] Netherton Syndrome Nevus, Sebaceous of Jadassohn [C16.131.077.633] Nevus, Sebaceous of Jadassohn Oculocerebrorenal Syndrome [C16.131.077.662] Oculocerebrorenal Syndrome Orofaciodigital Syndromes [C16.131.077.676] Orofaciodigital Syndromes Pallister-Hall Syndrome [C16.131.077.690] Pallister-Hall Syndrome Pentalogy of Cantrell [C16.131.077.696] Pentalogy of Cantrell POEMS Syndrome [C16.131.077.703] POEMS Syndrome Polycystic Kidney Diseases [C16.131.077.717] Polycystic Kidney Diseases Prader-Willi Syndrome [C16.131.077.730] Prader-Willi Syndrome Prolidase Deficiency [C16.131.077.735] Prolidase Deficiency Proteus Syndrome [C16.131.077.740] Proteus Syndrome Prune Belly Syndrome [C16.131.077.745] Prune Belly Syndrome Rubella Syndrome, Congenital [C16.131.077.790] Rubella Syndrome, Congenital Rubinstein-Taybi Syndrome [C16.131.077.804] Rubinstein-Taybi Syndrome Short Rib-Polydactyly Syndrome [C16.131.077.850] Short Rib-Polydactyly Syndrome Silver-Russell Syndrome [C16.131.077.855] Silver-Russell Syndrome Smith-Lemli-Opitz Syndrome [C16.131.077.860] Smith-Lemli-Opitz Syndrome Smith-Magenis Syndrome [C16.131.077.879] Smith-Magenis Syndrome Sotos Syndrome [C16.131.077.889] Sotos Syndrome Trichothiodystrophy Syndromes [C16.131.077.899] Trichothiodystrophy Syndromes Trisomy 13 Syndrome [C16.131.077.919] Trisomy 13 Syndrome Trisomy 18 Syndrome [C16.131.077.929] Trisomy 18 Syndrome Waardenburg Syndrome [C16.131.077.938] Waardenburg Syndrome Weill-Marchesani Syndrome [C16.131.077.941] Weill-Marchesani Syndrome Wolf-Hirschhorn Syndrome [C16.131.077.944] Wolf-Hirschhorn Syndrome Zellweger Syndrome [C16.131.077.970] Zellweger Syndrome DISEASES Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] Congenital, Hereditary, and Neonatal Diseases and Abnormalities Infant, Newborn, Diseases [C16.614] Infant, Newborn, Diseases Amniotic Band Syndrome [C16.614.042] Amniotic Band Syndrome Anemia, Neonatal [C16.614.053] Anemia, Neonatal Asphyxia Neonatorum [C16.614.092] Asphyxia Neonatorum Birth Injuries [C16.614.131] Birth Injuries Colic [C16.614.166] Colic Congenital Bone Marrow Failure Syndromes [C16.614.183] Congenital Bone Marrow Failure Syndromes Congenital Hyperinsulinism [C16.614.200] Congenital Hyperinsulinism Cystic Fibrosis [C16.614.213] Cystic Fibrosis Epilepsy, Benign Neonatal [C16.614.258] Epilepsy, Benign Neonatal Erythroblastosis, Fetal [C16.614.304] Erythroblastosis, Fetal Hernia, Umbilical [C16.614.378] Hernia, Umbilical Hydrophthalmos [C16.614.438] Hydrophthalmos Hyperbilirubinemia, Neonatal [C16.614.451] Hyperbilirubinemia, Neonatal Hyperostosis, Cortical, Congenital [C16.614.465] Hyperostosis, Cortical, Congenital Ichthyosis [C16.614.492] Ichthyosis Infant, Premature, Diseases [C16.614.521] Infant, Premature, Diseases Meconium Aspiration Syndrome [C16.614.580] Meconium Aspiration Syndrome Mobius Syndrome [C16.614.595] Mobius Syndrome Neonatal Abstinence Syndrome [C16.614.610] Neonatal Abstinence Syndrome Neonatal Sepsis [C16.614.627] Neonatal Sepsis Nystagmus, Congenital [C16.614.643] Nystagmus, Congenital Ophthalmia Neonatorum [C16.614.677] Ophthalmia Neonatorum Persistent Fetal Circulation Syndrome [C16.614.694] Persistent Fetal Circulation Syndrome Rothmund-Thomson Syndrome [C16.614.760] Rothmund-Thomson Syndrome Sclerema Neonatorum [C16.614.810] Sclerema Neonatorum Severe Combined Immunodeficiency [C16.614.815] Severe Combined Immunodeficiency Syphilis, Congenital [C16.614.868] Syphilis, Congenital Thanatophoric Dysplasia [C16.614.890] Thanatophoric Dysplasia Thrombocytopenia, Neonatal Alloimmune [C16.614.899] Thrombocytopenia, Neonatal Alloimmune Toxoplasmosis, Congenital [C16.614.909] Toxoplasmosis, Congenital Vitamin K Deficiency Bleeding [C16.614.940] Vitamin K Deficiency Bleeding Wolman Disease [C16.614.947] Wolman Disease

Mobius Syndrome - Preferred

Concept UI	M0008126
Scope note	A syndrome of congenital facial paralysis, frequently associated with abducens palsy and other congenital abnormalities including lingual palsy, clubfeet, brachial disorders, cognitive deficits, and pectoral muscle defects. Pathologic findings are variable and include brain stem nuclear aplasia, facial nerve aplasia, and facial muscle aplasia, consistent with a multifactorial etiology. (Adams et al., Principles of Neurology, 6th ed, p1020)
Preferred term	Mobius Syndrome
Entry term(s)	Congenital Oculofacial Paralysis, Moebius Congenital Ophthalmoplegia and Facial Paresis Mobius Syndromes Moebius Congenital Oculofacial Paralysis Moebius Sequence Moebius Spectrum Moebius Syndrome Moebius Syndromes Möbius Sequence