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DO Term Detail DO ID: DOID:2106

Disease Ontology Information
DO ID DOID:2106
Alter ID
Name myotonia congenita
Name Space
Definition A muscle tissue disease that is characterised by slow muscle relaxation associated with hyperexcitation of the muscle fibres. []
Comment OMIM mapping confirmed by DO. [SN].
Created By
Creation Date
IS A DOID:66
IS OBSOLETE
IS TRANSITIVE
Synonym Thomsen disease EXACT []
Thomsen's disease EXACT [CSP2005:1849-6776]
Subset DO_rare_slim
Relationship
Xref ICD9CM:359.22
MSH:D009224
NCI:C84912
NORD:http
OMIM: 160800
OMIM: 255700
ORDO:614
UMLS_CUI:C0027127
Associated with this Disease Ontology and this descendants
Organism Species Resources Count
Strain / DNA
Ciona intestinalis 19 / 33
C. elegans 6 / 0
Tree View
At 'A / B resources (genes)' of the tree view, 'A' is a number of resources (genes) associated with this DO directly.'B' is the sum of resources (genes) associated with this DO and its descendants. If 'B' is bigger, it might take a lot of time to display the link of 'B'.
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