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Parent Node:
expandnervous system disorder (MONDO:0005071)
..Starting node
..expanddiplegia of upper limb ()

       Child Nodes:



 Sister Nodes: 
..expandautoimmune disease of the nervous system ()
..expandBalint syndrome ()
..expandBarre-Lieou syndrome ()
..expandcentral nervous system disease ()
..expandcerebral disease with cataract ()
..expandcomplex neurodevelopmental disorder ()
..expandcongenital nervous system disorder ()
..expandcranial nerve neuropathy ()
..expanddevelopmental disability ()
..expanddiplegia of upper limb ()
..expanddrug-induced akathisia ()
..expanddrug-induced dyskinesia ()
..expandgenetic nervous system disorder ()
..expandGerstmann syndrome ()
..expandidiopathic recurrent stupor ()
..expandinfectious disease of the nervous system ()
..expandinherited nervous system cancer-predisposing syndrome ()
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..expandmovement disorder ()
..expandneonatal brainstem dysfunction ()
..expandnervous system injury ()
..expandnervous system neoplasm ()
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..expandsymmetrical thalamic calcifications ()
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..expandWallerian degeneration ()
..expandWorster-Drought syndrome ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:4618
Name:diplegia of upper limb
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:diplegia of upper limbs; diplegia, upper
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes: MYOC;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal