Search Ontology:
Human Disease

Moebius syndrome

Term ID
DOID:13501
Synonyms
  • Mobius syndrome
  • Moebius congenital oculofacial paralysis
  • Oromandibular-limb hypogenesis spectrum
Definition
A facial nerve disease characterized by congenital, uni- or bilateral, non-progressive facial weakness and limited abduction of the eye(s). (2)
References
  • GARD:8549
  • ICD10CM:Q87.0
  • MESH:D020331
  • MIM:157900
  • NCI:C84893
  • SNOMEDCT_US_2023_03_01:89444000
  • UMLS_CUI:C0221060
Ontology
Human Disease   ( DOID:13501 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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