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DO Term : Moebius syndrome [DOID:13501] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A facial nerve disease characterized by congenital, uni- or bilateral, non-progressive facial weakness and limited abduction of the eye(s).

synonyms:
ICD10CM:Q87.0,
UMLS_CUI:C0221060,
157900,
SNOMEDCT_US_2023_03_01:89444000,
MESH:D020331,
OMIM:157900,
Mobius syndrome,
GARD:8549,
Oromandibular-limb hypogenesis spectrum,
Moebius congenital oculofacial paralysis,
NCI:C84893

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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