Hearing Loss Disease Portal


 
Switch to table view
Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandAbnormalities, Multiple (D000015)
Parent Node:
expandFacial Nerve Diseases (D005155)
Parent Node:
expandInfant, Newborn, Diseases (D007232)
..Starting node
..expandMobius Syndrome (D020331)

       Child Nodes:
........expandCongenital facial diplegia (C531747)
........expandMoebius axonal neuropathy hypogonadism (C535806)
........expandMoebius syndrome 1 (C535807)
........expandMyopathy, congenital nonprogressive with Moebius and Robin sequences (C536102)



 Sister Nodes: 
..expandAmniotic Band Syndrome (D000652) Child3
..expandAnemia, Neonatal (D000751) Child2
..expandAsphyxia Neonatorum (D001238) Child1
..expandBirth Injuries (D001720) Child1
..expandCarnitine Palmitoyltransferase II Deficiency, Lethal Neonatal (C563463)
..expandCongenital Hyperinsulinism (D044903) Child2
..expandCutis Laxa-Marfanoid Syndrome (C563639)
..expandCystic Fibrosis (D003550) Child4
..expandDevelopmental Delay, Epilepsy, and Neonatal Diabetes (C565253)
..expandDiabetes Mellitus, Transient Neonatal, 1 (C563322)
..expandDiabetes Mellitus, Transient Neonatal, 2 (C563672)
..expandEpilepsy, Benign Neonatal (D020936) Child13
..expandErythroblastosis, Fetal (D004899) Child7
..expandHernia, Umbilical (D006554) Child6
..expandHydrophthalmos (D006871)
..expandHyperbilirubinemia, Neonatal (D051556) Child4
..expandHypercalcemia, Idiopathic, of Infancy (C562581)
..expandHyperglycinemia, Transient Neonatal (C562672)
..expandHyperostosis, Cortical, Congenital (D006958) Child6
..expandHyperparathyroidism, Neonatal Severe Primary (C563375)
..expandHypoglycemia, Neonatal, Simulating Foetopathia Diabetica (C565484)
..expandIchthyosis (D007057) Child66
..expandInfant, Premature, Diseases (D007235) Child14
..expandMeconium Aspiration Syndrome (D008471)
..expandMobius Syndrome (D020331) Child4
..expandNeonatal Abstinence Syndrome (D009357)
..expandNystagmus, Congenital (D020417) Child17
..expandOphthalmia Neonatorum (D009878)
..expandPersistent Fetal Circulation Syndrome (D010547) Child1
..expandRothmund-Thomson Syndrome (D011038) Child5
..expandSclerema Neonatorum (D012593)
..expandSevere Combined Immunodeficiency (D016511) Child22
..expandSyphilis, Congenital (D013590)
..expandThanatophoric Dysplasia (D013796) Child8
..expandThrombocytopenia, Neonatal Alloimmune (D054098)
..expandToxoplasmosis, Congenital (D014125)
..expandVitamin K Deficiency Bleeding (D006475)
..expandWolman Disease (D015223) Child2
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:7351
Name:Mobius Syndrome
Definition: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)
Alternative IDs:
ParentIDs:MESH:D000015|MESH:D005155|MESH:D007232
TreeNumbers:C10.292.300.825 |C16.131.077.578 |C16.614.595
Synonyms:Congenital Oculofacial Paralysis, Moebius |Congenital Ophthalmoplegia and Facial Paresis |Möbius Sequence |Mobius Syndromes |Moebius Congenital Oculofacial Paralysis |Moebius Sequence |Moebius Spectrum |Moebius Syndrome |Moebius Syndromes
Slim Mappings:Congenital abnormality|Infant-newborn disease|Nervous system disease
Reference: MedGen: D020331
MeSH: D020331
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants