FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Moebius syndrome ID (Ontology) DOID:13501 (Human Disease)
Definition A facial nerve disease characterized by congenital, uni- or bilateral, non-progressive facial weakness and limited abduction of the eye(s).
Also Known As "Mobius syndrome" ; "Moebius congenital oculofacial paralysis" ; "Oromandibular-limb hypogenesis spectrum"
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Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
cranial nerve disease           |
 |__facial nerve disease________|
                                Moebius syndrome
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Is a autosomal dominant disease
facial nerve disease
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Synonyms
  • "Mobius syndrome" EXACT
    "Moebius congenital oculofacial paralysis" EXACT
    "Oromandibular-limb hypogenesis spectrum" EXACT
Secondary IDs
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GARD:8549
ICD10CM:Q87.0
MESH:D020331
MIM:157900
NCI:C84893
SNOMEDCT_US_2023_03_01:89444000
UMLS_CUI:C0221060