Mobius Syndrome
Disease ID: disease_node_10509
Connections displayed (default: 10).
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| Dbxref | GARD:8549, ICD10CM:Q87.0, MESH:D020331, MIM:157900, NCI:C84893, SNOMEDCT_US_2023_03_01:89444000, UMLS_CUI:C0221060 |
|---|---|
| Subclassof | DOID_0050736, DOID_1756 |
| Data Source | DOID, MESH |
| Synonyms | Mobius syndrome, Moebius congenital oculofacial paralysis, Oromandibular-limb hypogenesis spectrum |
| Mesh Id | D020331 |
| Mesh Label | Mobius Syndrome |
| Mesh Subclassof | D000015, D005155, D000093922, D007232 |
| Doid Label | Moebius syndrome |
| Doid Description | A facial nerve disease characterized by congenital, uni- or bilateral, non-progressive facial weakness and limited abduction of the eye(s). OMIM mapping confirmed by DO. [SN]. |
| Has Symptom | SYMP_0000094 |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_10509 |
| Doid Id | DOID_13501 |
| Label | Mobius Syndrome |
- Outgoing r'ship
HAS_SYMPTOMto/from Muscle Weakness(ID:disease_node_9835;disease_node_21022) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)